Equipment Servicing

AxisCare Health Logistics, Inc. (Axis) is a Puerto Rico–based healthcare distributor and service provider founded in 1986. Operating through eight specialized divisions, the company serves over 1,200 commercial clients and 217,000 patients through contracts with major health insurers (PMC, MMM, Humana, First Medical, Triple S, Mapfre, MCS). AxisMed distributes 147 product lines from major manufacturers including 3M, Abbvie, Baxalta, Baxter, Coloplast, ConvaTec, Covidien, Drive Medical, Dynarex, Hill-Rom, Hospira, KiMobility, Prodigy, Respironics, Stryker, and Welch Allyn, with over 8,000 SKUs in inventory and 24-hour island-wide delivery. Axis Health provides home-based medical equipment management and durable medical equipment (DME) under Medicare and Medicaid; services include diabetic supplies, medications, liquid oxygen, ventilation systems, complex rehabilitation equipment, enteral nutrition, and ostomy/urology products. Axis Biotech specializes in equipment maintenance and repair for durable medical equipment. Axis Mobility manufactures highly customized wheelchairs and assistive devices. Axis Ortho distributes Stryker orthopedic implants for knee and hip reconstruction. Axis Pharm provides direct-to-patient pharmaceutical delivery including respiratory therapy, anti-inflammatory, and dermatological products. Axis also offers third-party logistics (3PL) and distribution management services to healthcare manufacturers. The company maintains accreditation from Medicare/Medicaid Services Center, The Joint Commission, and the Puerto Rico Department of Health, with appropriate regulatory permissions from Puerto Rican government agencies.

ForTec Medical, Inc. is a national medical device distributor and clinical support provider specializing in on-demand surgical technology mobilization for hospitals, ambulatory surgery centers, and physician offices. Operating for over 35 years, the company maintains a fleet of approximately 1,350 devices across 30 major medical device categories, covering more than 180,000 cases annually across 10+ medical specialties. Core product offerings include UroNav targeted MRI/ultrasound biopsy systems, blue light cystoscopy systems for bladder cancer detection, Fujifilm Precision Arietta ultrasound systems with specialized probes for robotic partial nephrectomies, and high-frequency Holmium laser systems with virtual basket treatment modes for stone management. The company operates an extensive field support network of 550 skilled Clinical Technology Specialists across 48 states, providing preventative maintenance services, in-service training, and procedural case support. ForTec manages approximately 2,200 preventative maintenance events annually and offers solutions to eliminate facility maintenance costs and optimize operating room utilization. The company provides laser safety training courses, CE-accredited coursework through the Laser Education Portal, and clinical consulting services. Primary markets served include urology, general surgery, and other surgical specialties. Services include equipment delivery, setup, clinical support during procedures, training, and maintenance coordination.

HM Product Solutions, Ltd. is a Wisconsin-based supply chain management and contract services provider specializing in medical device support, industrial logistics, and product lifecycle management. The company operates as a B2B service provider offering kitting, assembly, packaging, contract manufacturing, procurement, warehousing, distribution, and reverse logistics. Core service lines include: notifications and tracking (production verification and standards compliance reporting); kitting and assembly (warranty recall kits, field upgrades, general subcontract kitting with lean manufacturing support and just-in-time delivery); print and media duplication (software duplication and binding services for field equipment maintenance and upgrades); procurement and supply chain management (parts sourcing, managed inventory, line-side delivery); and contract manufacturing (rapid prototyping and small-run production). The company maintains a centrally located warehouse and fulfillment center serving medical, industrial, high-technology, and retail sectors. HM's medical division focuses on complex medical device supply chain solutions, product recall management, and lean manufacturing principles. The company emphasizes comprehensive product lifecycle support from market introduction through obsolescence. Quality systems and compliance capabilities are noted on the site, though specific certifications (FDA, ISO 13485) are not explicitly detailed in the main pages.

Parmed Medical Distributors is a Puerto Rico-based medical device and infusion products distributor serving clinical practices and hospitals throughout the island. The company specializes in infusion technology, including IV supplies, volumetric and ambulatory infusion pumps (notably Baxter brand products), elastomeric pumps, and infusion lines. Beyond infusion solutions, Parmed distributes a broad range of general medical products and maintains specialized oncology product lines tailored for cancer care settings. The company emphasizes quality, integrity, and reliability as core operational values. Parmed provides biomedical services including maintenance and repair of medical equipment, leveraging a team of professional engineers with expertise in medical device servicing. The company operates exclusively in the B2B healthcare sector—clinical practices and hospital systems only—and does not maintain a retail storefront. Parmed is developing digital capabilities through a mobile app to enhance customer ordering and service accessibility. Based in Bayamón, Puerto Rico, the company serves the local healthcare market and demonstrates commitment to improving healthcare delivery within Puerto Rico.

Solmetex LLC is a dental water management and amalgam recycling solutions provider headquartered in Northborough, Massachusetts. Operating since 1996, the company offers an integrated family of brands—Solmetex®, Sterisil®, and DryShield®—that deliver end-to-end water safety, waterline monitoring, and environmental compliance for dental practices. Core products include chairside and central water filtration systems, waterline testing kits (FASTCheck15™ rapid testing), vacuum line cleaners (PowerScrub), isolation systems (DryShield), and amalgam collection/recycling containers. Solmetex provides turnkey amalgam collection, disposal, and recycling services with EPA Dental Amalgam Rule compliance support. The company operates My Solutions Center™, a digital platform enabling practitioners to manage water test results, print recycling shipping labels, obtain recycling certificates, and automate product subscriptions. Services include live customer support from Certified Water Specialists, staff training, and educational resources focused on dental water safety and biofilm prevention. The company serves dental practices, dental service organizations (DSOs), and international markets through distributor networks in Canada and Mexico. Solmetex emphasizes environmental stewardship by reducing mercury pollution and promoting sustainable water management practices in dentistry.

Millstone Medical Outsourcing LLC is a contract manufacturing and post-manufacturing services provider headquartered in Mississippi serving medical device manufacturers globally. Founded in 2000, the company specializes in packaging, testing, logistics, and quality assurance for completed medical devices. Core capabilities include: packaging and assembly with ISO Class 7 cleanroom operations; quality-critical inspection and validation engineering; finished goods distribution and reverse logistics management including bone and tissue storage with cold-chain capability; set building and loaner management for surgical instruments; and comprehensive in-house testing services. Testing portfolio encompasses bioburden, sterility, bacterial endotoxin, microbial identification, particulate analysis, cytotoxicity, sterilization validation (gamma and ethylene oxide), EO residual testing, preservative efficacy, peel strength, dye penetration, bubble emission, accelerated aging, and environmental monitoring. The company operates 276,000 square feet of facility space with a 25,000-square-foot ISO 17025-certified laboratory featuring a world-class BI sterility suite for EO sterilization validation. FDA-registered and ISO 13485:2016 certified. Serves 50+ customers worldwide, including top-10 orthopedic device manufacturers. Offerings include pre-validated packaging solutions, system integration services, pharma-device distribution, and ImplantBase platform. Primary markets: orthopedics, surgical devices, and robotic-assisted surgery equipment.

Maestro Logistics is a US-based commercialization and contract manufacturing partner for emerging and established medical device companies. The company provides end-to-end services including first article inspection, end-of-line manufacturing (packaging, labeling, kitting, assembly), pre-distribution inspection, warehousing and distribution, order fulfillment, field return processing, surgical kit and instrument cleaning, and loaner program management. The company operates a state-of-the-art facility with validated, automated systems and employs quality systems personnel with over 60 years of combined medical device industry experience. Leadership includes a lean six-sigma black belt who implements statistical process controls to ensure efficiency and accuracy. Maestro serves companies at all stages—from prototypes and first articles through high-volume production and post-market support. The company is ISO 13485:2016 certified, ASQ-, ASTM-, and AAMI-aligned, and maintains compliance with medical device regulatory requirements. Typical customers include new entrants with emerging technologies seeking outsourced manufacturing and logistics, and established OEMs looking to reduce overhead by outsourcing inspection, fulfillment, and returns processing.

KX Medical is an FDA-registered contract manufacturer of single-use, disposable medical devices located in Gallatin, Tennessee. Operating a 30,000 sq ft facility, the company specializes in precision converting and custom medical device manufacturing with 30+ years of industry experience. Core product lines include advanced wound care dressings, continuous glucose monitoring components, remote patient monitoring devices, PPE for patients and caregivers, and IV dressings. The company serves large OEMs and medical device startups with engineering-focused solutions. Manufacturing capabilities include multi-station converting processes up to 13 inches wide with hyper-tight tolerances, inline multi-color flexographic printing, water-based and UV ink processing, Cognex video-controlled registration, Videojet lot coding, and slitting/rewinding services. Equipment includes 9-station and 7-station Delta Flex Crusaders and 16-inch wide 5-color flexographic printing systems. Quality and regulatory credentials include ISO 13485:2016 certification, FDA registration as a contract manufacturer, cGMP compliance, and CFR 820 adherence. UL Registered Firm with Certificate #35765.230523. The company emphasizes strong supplier relationships and custom solutions tailored to customer specifications.

Riverpoint Medical is a Portland, Oregon-based medical device manufacturer founded in 1990, specializing in the design, development, and manufacturing of advanced surgical fibers, implantable textiles, and regenerative technologies. The company serves orthopedics, sports medicine, cardiovascular care, wound closure, veterinary, and dental markets with bioresorbable and non-absorbable sutures, custom fibers, and implantable materials. Operating with approximately 50 employees and $7.4 million in annual revenue, Riverpoint Medical combines in-house technology and rapid innovation capabilities with comprehensive services including custom design, private labeling, manufacturing, and regulatory support. The company positions itself as a full-service partner enabling healthcare device manufacturers and suppliers to efficiently bring surgical fiber and textile-based solutions to market.

Crest Ultrasonics Corp. is a privately held manufacturer of industrial ultrasonic cleaning equipment and solutions, headquartered in New Jersey. The company specializes in heavy-duty ultrasonic cleaners designed to remove complex contaminants including caked-on residues, rust, oils, films, and debris across diverse industrial applications. The product portfolio includes aqueous ultrasonic cleaning systems (from benchtop to room-sized consoles with wash/rinse/dry automation), solvent ultrasonic cleaning equipment for pre- and post-removal of organic contaminants, custom-engineered ultrasonic cleaning units, and proprietary Chem-Crest® ultrasonic cleaning solutions and powders. Primary markets served include medical device manufacturing, pharmaceuticals, semiconductors, metal fabrication, optics, healthcare facilities (surgical instrument cleaning), aerospace, automotive, electronics, firearms, cosmetics, and jewelry. The company operates a global distribution network across 15 countries through subsidiary companies and independent distributors, providing sales, service, and support infrastructure. Crest offers custom equipment design and manufacturing capabilities, repair and servicing, free ultrasonic cleaning consulting, and surface treatment solutions such as citric acid passivation (Chem-Crest ProPass) for stainless steel. The company emphasizes reliability, precision, speed, and safety in cleaning operations. Regulatory certifications and specific compliance details are not explicitly stated on the website.

Surgical Solutions is a procedural support and sterile processing services provider serving U.S. hospitals and surgical facilities. The company operates as a deeply embedded partner delivering comprehensive on-site support across operating rooms, endoscopy departments, and sterile processing departments (SPD). Service offerings include pre-operative instrument preparation, intraoperative surgical assistance, post-operative care, scope reprocessing, instrument repair, sterile processing leadership and consulting, vendor relationship management, capital equipment planning, and 24/7/365 on-site technician support. The company emphasizes process optimization, compliance adherence to industry standards (including Joint Commission), staff training and development, and efficiency improvements documented by case studies showing $1M in direct endoscopy savings, 70% increases in minimally invasive procedure volumes, and 95% reduction in unused surgical tray rates. Surgical Solutions employs a customized, collaborative approach to each facility's procedural and sterilization workflow challenges, with dedicated focus on patient safety, surgical team support, and operational reliability.

TouchPoint Medical is a global medical technology manufacturer specializing in ergonomic workstations, automated medication management systems, and point-of-care solutions for healthcare facilities. The company designs and manufactures medical carts, mounting systems (including proprietary AccessMount™ arms), and secure medication dispensing cabinets tailored for hospitals, surgery centers, dental practices, medical schools, simulation labs, and healthcare facilities across 20+ countries. Products enhance workflow efficiency, patient safety, and caregiver ergonomics in clinical settings including emergency departments, ICUs, operating rooms, patient rooms, and pharmacy environments. TouchPoint Medical operates manufacturing facilities in Florida, USA, with headquarters and customer support offices in Odessa, FL, and additional regional support centers in Belgium, UK, China, Nordic countries, Australia, and UAE. The company holds ISO 13485 certification and HIMSS GOLD seal status, demonstrating commitment to quality management systems and healthcare IT interoperability standards. Service offerings include site assessments, product trials, deployment, training, preventive maintenance, and 24/7 technical support across multiple languages and regions. The company serves thousands of healthcare professionals globally and emphasizes single-vendor solutions and technology refresh programs.

Crest Healthcare Supply is a healthcare equipment distributor serving 45,000+ healthcare locations across the United States. The company operates a 3,000+ square foot warehouse and maintains an inventory of 10,000+ products spanning durable medical equipment, furniture, consumables, and operational supplies. Product lines include nurse call and communication systems (featuring Inovonics pendants and Crest call cords), bed and room products, mobility and transfer solutions (wheelchairs, walkers, crutches), fall prevention and monitoring equipment, aids for daily living, clinical care solutions, lighting systems, personal protective equipment (gloves, masks), infection control products, and operational supplies. The company also offers equipment repair services on a flat-rate basis. Crest Healthcare Supply functions as a one-stop B2B medical supply distributor for hospitals, long-term care facilities, assisted living communities, and other healthcare settings, emphasizing reliable service and product availability.

MedSource Imaging is the leading independent third-party provider of refurbished Hologic mammography equipment and parts, serving US and international facilities. The company specializes in high-quality refurbished Hologic mammography systems including Selenia Dimensions, Selenia 2D, Genius 3D, Affirm, SecurView, and Horizon DXA systems, priced at approximately 50% below new equipment costs. MedSource maintains the largest independent inventory of Hologic mammography parts and systems, including detectors, X-ray tubes, CPUs, monitors, paddles, workstation components, and biopsy devices. The company's comprehensive refurbishment process includes full restoration, calibration, component replacement, and testing to ensure systems meet MSI standards and deliver optimal performance. Service capabilities include rapid repairs, preventative maintenance, on-site and remote diagnostics, installation, transport, relocation, and removal. MedSource offers same-day parts shipping, nationwide service with 24-hour repair response, remote detector mapping assistance, and expert engineering consultation for parts matching. The company also purchases used Hologic mammography, DXA, and C-arm systems for resale. All equipment includes warranty support and 100% customer satisfaction guarantees. Experienced technical team handles turn-key imaging solutions and provides expert Hologic equipment expertise. The company has installed systems across multiple facilities and maintains an extensive parts inventory ready for immediate shipment.

Gentech Biomedical is a Puerto Rico-based clinical laboratory equipment distributor and service provider with over 32 years of operational history. The company supplies hematology analyzers (Sysmex XS1000i, Cell Dyn Ruby refurbished units), microscopes (ACCU-SCOPE EXC Series, 3012-LED), centrifuges (LW Scientific E8, MX5), blood mixers, digital cell counters, bench-top incubators, temperature/data logging systems (LogTag recorders), NIST-calibrated thermometers, and reagents for major equipment brands including Sysmex and Cell Dyn. The company also provides autoclavable mechanical pipettes in various volumes and custom reagent solutions. Beyond equipment sales, Gentech offers comprehensive technical support services including equipment maintenance, preventative maintenance programs, flexible service contracts, and replacement unit deployment for facilities across Puerto Rico and the Caribbean. Support covers major diagnostic brands: Sysmex, Cell-Dyn, Siemens Clinitek, Medika, Thermo, Helmer, and Baxter/Dade. Operations are certified under ISO 9001:2015 quality management standards, ensuring consistent reliability and compliance. The company targets hospitals, clinical laboratories, and diagnostic institutions requiring cost-effective solutions without quality compromise.

Right Way Medical is a US-based medical device distributor specializing in infusion pumps, disposables, biomedical services, and asset-tracking software for post-acute healthcare providers. The company distributes volumetric and enteral feeding pumps from manufacturers including Fresenius Kabi (Agilia Connect), Amsino (Puggle), Smith Medical (CADD SOLIS VIP), and Eitan (Sapphire Multi-Therapy System). Beyond product distribution, Right Way Medical offers comprehensive biomedical repair and maintenance services for medical equipment. The company developed Right Track, a proprietary asset-tracking software platform designed to minimize human error and streamline inventory management and equipment compliance for healthcare facilities. Right Way Medical operates multiple regional offices across the United States (Arizona, Texas, Illinois, Georgia, Pennsylvania) and serves post-acute care settings, pharmacies, and specialty medical product companies. The company maintains partnerships with numerous leading medical device manufacturers and has built relationships with major healthcare organizations since at least 2014. Services are characterized by direct account management, responsive support, and customized solutions tailored to provider needs.

QMD is a full-service medical device contract manufacturer specializing in silicone and elastomeric components, precision subassemblies, and finished device manufacturing. The company serves original equipment manufacturers (OEMs) across cardiology, critical care, infusion therapy, and surgical/respiratory applications. QMD's core capabilities include end-to-end manufacturing from component design through finished-device assembly, custom molded silicone and polyisoprene components (tubing, seals, valves, stoppers, duckbills), device assembly in ISO Class 7 & 8 cleanrooms, and packaging/sterilization services (ETO and gamma sterilization). Product portfolio includes coronary and peripheral vascular catheters (PTCA, PTA, aspiration), urinary catheters, enteral feeding tubes, central venous catheters, invasive blood pressure monitoring systems, chest and wound drainage products, and custom fluid management/respiratory/surgical subassemblies. The company holds FDA approvals, CE marking, 510(k) clearances, and Canadian regulatory licenses. Manufacturing capabilities span component-level customization through validated NPI processes, with private labeling and branded product transformation services. QMD operates Class 7 & 8 ISO-certified assembly facilities and provides comprehensive engineering and regulatory support to facilitate market entry for medical devices.

Wassenburg Medical B.V. is a global specialist in automated endoscope reprocessing systems and solutions since 1984. The company designs, manufactures, and distributes comprehensive endoscope cleaning, disinfection, drying, storage, and traceability systems for hospitals and clinics worldwide. Their flagship product, the WASSENBURG® WD4200, represents an intelligent automated solution for complete endoscope reprocessing workflows. Wassenburg offers a complete "total solution" encompassing pre-cleaning, washing and high-level disinfection, drying and conditioning, transport systems, and full traceability/tracking capabilities to ensure infection control and regulatory compliance. The company maintains direct sales offices and distribution partnerships across 35 countries, including North America, Europe, Asia-Pacific, and Latin America. Wassenburg is relocating to a new facility in Elst, Netherlands in 2026. The company serves hospitals, surgery centers, gastroenterology clinics, and endoscopy facilities. Products comply with medical device regulations and infection control standards. Wassenburg emphasizes user-friendly, efficient, and innovative reprocessing processes to support infection-free patient treatment and safe endoscope handling.

Advanced Endoscopy Devices, Inc. (AED) is a manufacturer and independent service provider of endoscopy equipment and surgical instruments. Founded in 1985, AED specializes in manufacturing innovative endoscopic video systems, cystoscopes, laparoscopic instruments, and arthroscopy equipment for urology, general surgery, and minimally invasive procedures. The company operates one of the largest endoscopy repair and servicing operations in the industry, with European factory-trained master technicians offering rapid turnaround (typically 24 hours) and a 99% success rate. AED repairs all major brands of endoscopic instruments with in-house parts manufacturing and inventory. Products include the EndoPro-Cam series (Primo, Master, Elite, and 3D visualization systems) and high-definition cystoscopes. The company is ISO 13485 certified, GSA-listed, and serves hospitals, surgical centers, and urological practices seeking cost-effective alternatives to manufacturer repairs—typically 30–50% below manufacturer pricing—without compromising quality or performance.

Miller Technical Services (MTS) is a contract medical device manufacturer and service provider specializing in complex electro-mechanical device manufacturing, assembly, and support for Class I, II, and III medical devices. The company serves medical device companies, inventors, private equity firms, and pharmaceutical organizations. Core capabilities include project management, contract manufacturing and assembly, supply chain management, automated systems integration, engineering support, production assembly, testing, packaging, device history record maintenance, and warranty parts depot services. MTS operates a service depot for sourcing, purchasing, warehousing, and shipping of new and refurbished devices and replacement parts. The company manages a vetted supply chain encompassing electronics, machining, casting, forging, and injection molding. FDA registered and ISO 13485 certified, MTS positions itself as a full-lifecycle partner from concept through production and post-market support, with ERP systems integrating financial, manufacturing, purchasing, and inventory management.

Coghlin Companies, Inc. is a fourth-generation contract manufacturing and engineering services company (founded 1885) specializing in the design, engineering, and precision manufacturing of complex capital equipment and medical devices. Based in Westborough, Massachusetts, with ~480 employees and $159.9M annual revenue, the company serves medical life sciences, semiconductor, robotics, and industrial sectors. Core capabilities include product engineering, design for manufacturability (DFM), prototyping, printed circuit board assembly, total system integration, and global supply chain fulfillment. Notable achievements include manufacturing 10,000 ventilators during COVID-19. Coghlin operates both industrial (Columbia Tech) and medical (Cogmedix) divisions, providing end-to-end commercialization services from concept through scalable manufacturing and aftermarket support.

Pro Scope Systems is an ISO 13485-certified provider of endoscopy equipment and repair services with over 35 years of industry experience. The company specializes in endoscope repair for flexible and rigid scopes from major manufacturers including Olympus, Pentax, Storz, Fujinon, and Stryker, utilizing OEM-equivalent parts to restore equipment to like-new performance standards. The company operates a comprehensive service model including fast, reliable repairs backed by warranty coverage and free loaner scopes to minimize facility downtime. Pro Scope Systems maintains an extensive inventory of pre-owned and refurbished endoscopes, each undergoing a rigorous 50-point inspection and testing process to meet or exceed OEM standards, offering cost savings of up to 60% compared to new equipment purchases. The company also operates a buy-back program allowing healthcare facilities to trade in or sell unused endoscopy equipment. Pro Scope Systems serves hospitals, medical practices, and veterinary clinics globally, emphasizing customer-centric service, competitive pricing, and rapid turnaround times. The company actively seeks qualified international distributors to expand its market reach.

Brooks Automation is a global leader in automation solutions for the semiconductor and manufacturing industries, founded in 1978 and headquartered in Chelmsford, Massachusetts. The company specializes in innovative hardware, software, and services designed to enhance manufacturing efficiency, throughput, yield, and cost of ownership. Their automation systems focus on transport, handling, storage, and purity control. With over 1,000 employees worldwide, Brooks Automation has established itself as a trusted partner for major players in process equipment and device manufacturing. The company emphasizes mechatronics, advanced motion and vision control, and intelligent software to deliver reliable and scalable solutions. Brooks continues to expand into laboratory automation and emerging markets, maintaining a strong commitment to customer success and value creation.

Polo Custom Products is a contract manufacturing specialist founded in 1947, providing industrial sewing, RF welding, thermoforming, and supply chain management services to original equipment manufacturers (OEMs) across medical, military and government, fire and safety, and powersports industries. The company designs, engineers, and manufactures custom soft goods including medical bags, urine and drainage bags, safety harnesses, strap assemblies, carrying cases, backpacks, and equipment covers. Core capabilities include custom industrial sewing of foam, film, and fabric materials; Radio Frequency (RF) sealing and dielectric welding for sealed applications such as emergency oxygen bags and air bladders; and thermoforming of foam, fabric, and film. Additional services encompass product concept development, design engineering, raw materials sourcing, supply chain and materials management, quality assurance controls, branding, assembly, packaging, warehousing, and international logistics. The company serves OEMs requiring contract manufacturing solutions to consolidate vendor relationships and reduce operational complexity. Polo Custom Products maintains an established reputation for quality, responsive customer service, and technical expertise across multiple manufacturing disciplines, positioning itself as a full-service partner for complex soft goods production.

PEMCO, Inc. is an American manufacturer of precision reusable cardiothoracic surgical instruments, founded in 1946 as a manufacturing and machine shop facility in Cleveland, Ohio, with surgical instrument design and production since 1955. The company specializes in cardiovascular surgical instruments, including ostial perfusion cannulas, cardiac suckers, and the Rultract® retractor line. PEMCO manufactures precision reusable instruments designed to reduce operating room costs by minimizing disposable consumption, lowering medical waste, reducing environmental impact, and decreasing occupational exposure risks. The company operates as a third-generation family business with state-of-the-art manufacturing and machining capabilities. Beyond medical instruments, PEMCO serves industrial clients and provides custom manufacturing to meet specific customer specifications. The company offers comprehensive service and refurbishment programs for all manufactured products, extending product lifecycle and value. PEMCO is the exclusive authorized service facility for Rultract® retractor products, offering component refurbishment and full-system refurbishment options. The company's instruments are designed with ergonomic and environmental considerations for operating room integration.

Berkeley Biologics is a tissue bank and contract manufacturer specializing in human allograft implants for orthopedics, spine, sports medicine, trauma, dental, and wound care. The company has 35+ years of expertise in tissue processing and transplantation. Core product lines include D-FIBER (demineralized cortical fiber matrix for bone regeneration), AcelloDerm (pre-hydrated acellular dermal matrix), AltiPly (lyophilized placental membrane for wound care), InteguPly (acellular dermis for sports medicine and wound repair), and TranZgraft (processed allograft tissues including tendons and ligaments for sports medicine). All products undergo rigorous donor screening, communicable disease testing, and quality assurance per AATB and FDA standards. Berkeley Biologics processes tissues using proprietary methods including low-dose e-beam irradiation and gamma sterilization to achieve sterility assurance level (SAL) of 10-6, while preserving native matrix structure, collagen integrity, and endogenous growth factors (BMP, FGF, IGF-1, PDGF, TGF-β). The company operates state-of-the-art manufacturing facilities in Northern California and offers turnkey contract manufacturing, private-label allograft opportunities, custom implant development, engineering and validation support, and inventory management services. Regulatory compliance includes FDA registration (21 CFR Parts 820 and 1271), AATB accreditation, and tissue bank licensure in California, Florida, Maryland, New York, Delaware, Illinois, Oregon, and Canada (CTO registration). The company serves surgeons, hospitals, and surgical centers across multiple specialties.

Mendtronix is a San Diego-based third-party logistics (3PL) and operational services provider specializing in ISO 13485:2016-certified, FDA-registered supply chain solutions for medical device manufacturers and other regulated industries. With 27+ years of experience, the company offers contract assembly, kitting and packaging, secure warehousing, returns/reverse logistics management, RMA repair and reconditioning, technical services, Amazon FBA preparation, and order fulfillment from its US facility. Mendtronix supports Class I and Class II medical devices on build-to-order and build-to-stock bases, while also serving consumer goods, electronics, and industrial manufacturers. The company delivers structured workflows, complete traceability, component-level inspection, production accuracy (97%), and responsive support designed to scale with client growth and operational complexity.

National Distribution & Contracting, Inc. (NDC) is a healthcare supply chain solutions provider headquartered in Nashville, Tennessee. The company operates through multiple business segments: a B2B distributor and manufacturer solutions division offering market intelligence platforms, supply chain optimization, 3PL services, master distribution, and business management solutions including contract and rebate processing; and Preferred Medical, a national wholesale distributor of medical supplies and equipment for infusion therapy and post-acute care markets. NDC serves over 450 manufacturer partners, 1,500 distributor and integrated delivery network (IDN) partners, and provides access to products for 6,800+ healthcare providers. Core capabilities include proprietary data analytics for competitive intelligence, group purchasing organization (GPO) services, vaccine buying groups, pharmaceutical sourcing for generic injectables, talent development programs, and marketing solutions. Preferred Medical specializes in distribution of IV therapy products, infusion pump services including repair, maintenance and rental, Wolf-Pak® brand consumables, and post-acute care supplies to home infusion pharmacies, infusion centers, ambulatory clinics, and long-term care facilities. The company provides scalable warehousing, fulfillment, and regulatory support infrastructure. NDC operates as a master distributor enabling manufacturers to access wide provider networks and independent distributors to leverage shared scale and national brand access.

American I.V. Products, Inc. (AIV) is a medical equipment supplier specializing in infusion pump solutions, replacement parts, and healthcare facility infrastructure. The company distributes refurbished and patient-ready IV pumps from major manufacturers, offering cost-effective alternatives to new equipment. AIV maintains an extensive inventory of OEM-compatible infusion pump replacement parts, cables, and sensors for leading brands. The company also manufactures and distributes PowerMATE® brand medical power taps and relocatable power distribution units designed for healthcare environments, including models with locking outlet covers and dual-rated special purpose configurations. AIV provides equipment repair and servicing capabilities, including calibration and maintenance support. The company operates a refurbishment program, accepting obsolete infusion pump inventory from healthcare facilities and hospitals in exchange for cash, then reselling patient-ready refurbished units. AIV serves major health systems and hospital networks, with documented relationships including CommonSpirit Health. The company maintains service expertise across multiple infusion pump platforms and offers technical support alongside product sales. Operations include parts warehousing, equipment servicing, and distribution logistics for the hospital and healthcare facility market.

Mach Medical is an orthopedic contract manufacturer (CMO) specializing in High Velocity Manufacturing and High Velocity Engineering Transfer processes. The company serves OEM partners by designing, engineering, and manufacturing orthopedic implants with flexible, low-setup production capabilities. Mach's manufacturing platform enables economical production runs as small as one unit with near-zero machine setup time between product runs, supported by automated inspection and documentation systems. The company offers two primary inventory-reduction models: (1) direct supply of orthopedic implants with 3-week lead times in any order quantity, reducing customer warehouse inventory by up to 70%, and (2) case-templated, surgery-specific manufacturing that reduces overall OEM inventory (warehouse plus field deployment) by up to 85%, from 12+ months to 2–3 months. High Velocity Engineering Transfer leverages Siemens and Microsoft platforms with automated CNC programming and QMS documentation to compress engineering-to-production timelines to 3 months or less, potentially shortening time-to-market by 1–2 years versus traditional approaches. Mach Medical serves orthopedic OEMs and healthcare systems seeking supply chain agility, capital efficiency, and accelerated product commercialization.

ATMOS Medizintechnik is a German-headquartered medical technology manufacturer with over 130 years of expertise and 300+ employees worldwide. The company develops and supplies medical suction systems, ENT (otolaryngology) workstations and treatment units, gynecology diagnostic and therapeutic equipment, and flexible endoscopy systems for swallowing diagnostics (FEES). ATMOS maintains 15 subsidiaries and approximately 70 national agencies internationally, serving hospitals, clinics, private practices, and homecare providers. Core product lines include electrical and pneumatic suction devices (ATMOS and MEDAP brands), ENT treatment units (C 21/C 31 Economy series, S 61 CORIAN), flexible HD video endoscopes (ATMOS Scope), ENT case management software, and gynecology solutions focused on cervical cancer diagnosis and treatment. The company emphasizes intuitive design, high infection control standards, workflow optimization, and user safety. ATMOS offers comprehensive post-sale services including technical support, repairs, maintenance, spare parts supply, and device modernization. Products are designed for clinical environments with emphasis on ease of use and reliability for end-users. The company maintains ISO and CE certifications typical of European medical device manufacturers and distributes globally through both direct channels and regional representatives.

Ensera (formerly SteriPack) is a global medical device design and manufacturing contract services organization with operations in Europe, North America, and Asia. The company specializes in end-to-end design, engineering, and manufacturing of complex medical devices and pharmaceutical products across drug delivery, orthopedics, surgical devices, and diagnostics. Core capabilities include device design and product development (research, strategy, human factors, industrial design, UX/UI, engineering, electronics/software, prototyping); design-for-manufacture optimization; contract manufacturing including device manufacturing and assembly; sterile barrier system packing and kitting; sterilization management; cleanroom clean-pack-sterilize services; and primary/secondary packing for vials and combination products. The company also provides contract pharmaceutical services including final assembly, kitting, and secondary packing for combination products. Ensera operates GMP-licensed, ISO-certified cleanroom facilities across multiple continents and serves pharmaceutical organizations and medical device manufacturers targeting global markets. Regulatory credentials include FDA inspection compliance, ISO certification, GMP licensure, and EcoVadis ESG assessment. The Lakeland, Florida facility (formerly SteriPack USA) provides contract manufacturing and packing services for North American markets. The company emphasizes supply chain management, project management, quality assurance, and infrastructure support services.

Surgical Instrument Service Company (SIS) is a specialized medical equipment repair and maintenance provider headquartered in Glendale Heights, Illinois. Founded in 1971 by a former operating room nurse, SIS brings over 50 years of industry experience to healthcare facility partnerships nationwide. The company delivers comprehensive repair and maintenance services for surgical instruments, endoscopes, video systems, power equipment, and ultrasound transducers, with emphasis on extending instrument life through refurbishment rather than replacement. SIS maintains brand-neutral servicing capabilities for all manufacturers, including legacy and obsolete equipment models. Core service offerings include instrumentation repair, endoscope overhauls and insulation testing, video system repairs, power equipment servicing, and onsite support via mobile Instrument Care Units. The company provides customized training and process evaluation services, alongside cost-reduction programs including capitated agreements, asset management, shared-risk models, and time-and-material contracts. SIS prioritizes operational efficiency, patient safety, and long-term client partnerships with hospitals and healthcare systems.

Jubilant HollisterStier (JHS) is a contract manufacturing organization (CMO) specializing in sterile pharmaceutical manufacturing services. Based in Spokane, Washington, the company provides comprehensive sterile fill-finish, lyophilization, inspection, and packaging services for pharmaceutical and biopharmaceutical clients globally. JHS operates advanced manufacturing equipment including state-of-the-art lyophilizers with full-line integration, automation, and -55°C cold shelf loading capabilities, alongside steam-in-place systems. The company offers end-to-end inspection and packaging solutions with multiple inspection modalities and custom packaging options to support product distribution worldwide. JHS also provides comprehensive support services designed to ensure regulatory confidence and manufacturing excellence. The company serves pharmaceutical manufacturers seeking flexible, collaborative partnerships to accelerate time-to-market while maintaining quality standards. By 2026, JHS projects capacity to serve over 300 million patients annually. The company is recognized as the largest manufacturer by employee count in the Spokane area and won the Association of Washington Businesses Manufacturer of the Year Award (2024) and Manufacturing Excellence Award for Operational Excellence (2025), as well as the Greater Spokane Valley Chamber of Commerce Manufacturer of the Year (2024).

Scientific Molding Corporation (SMC) Ltd. is an FDA-registered, ISO 13485-certified contract manufacturer serving the medical device, diagnostic, and pharmaceutical industries for over 35 years. The company specializes in complex medical device manufacturing from concept through commercialization, including injection molding (thermoplastic and silicone), assembly, packaging, and global fulfillment. SMC offers end-to-end capabilities spanning design and engineering, supply chain management, quality and regulatory support, and manufacturing of single-use and disposable medical devices. The company manufactures innovative autoinjector platforms customizable to drug formulations, along with custom surgical tools, biopsy devices, diagnostic cartridges, and combination products. Pharma services include development services, analytical services, sterile fill-finish, commercial manufacturing, and comprehensive packaging and labeling solutions. SMC maintains FDA-registered facilities and holds ISO 13485 certification across all manufacturing operations. The company serves leading medtech, diagnostic, and pharmaceutical partners with capabilities in rapid prototyping, tech transfer, scalability, and risk reduction. Services encompass program management, supply chain optimization, and support from early-stage development through market distribution.

Perry Baromedical Corporation is the leading full-line manufacturer of hyperbaric oxygen therapy (HBO) systems in North America, with over 60 years of FDA-approved manufacturing experience. The company designs, manufactures, installs, and services monoplace, dualplace, and multiplace hyperbaric chambers for hospital, clinic, and specialty medical applications. Product lines include the Sigma 34, 36, and 40 monoplace chambers; the Sigma 40-II dualplace chamber; and the Sigma Multiplace Series (2–18 occupancy configurations), as well as the premium Sigma Elite single-user chamber. All systems are FDA-approved and designed for clinical hyperbaric oxygen therapy treatments. Perry offers complementary facility design services for chamber installation, replacement parts and accessories, and proprietary Perry Elite EMR software for patient management. The company provides comprehensive technical support, equipment servicing, calibration, and a certified 40-hour Hyperbaric Operator training course. Perry serves hospitals, wound care centers, military installations, and specialty medical facilities globally, with demonstrated regulatory compliance and a track record in clinical hyperbaric medicine.

HealthTronics is a specialized urology equipment and service provider serving over 1,500 physicians and 2,000 healthcare facilities nationwide. The company specializes in lithotripsy (shockwave), laser, and ureteroscopy solutions for kidney stone disease management. HealthTronics offers a comprehensive stone management platform including extracorporeal shock wave lithotripsy (ESWL) systems, laser lithotripsy equipment, single-use ureteroscopes, and consumables for ureteroscopic procedures. The company operates under a physician investment model, providing joint venture and partnership solutions to urologists and hospital systems seeking capital-efficient kidney stone treatment programs. Core service capabilities include equipment rental, maintenance, repair, and technical support through field engineers deployed nationally. HealthTronics emphasizes operational management of medical technology, quality assurance, compliance support, and process optimization. The company positions itself as both a product supplier and operational solutions provider, enabling practices and facilities to improve financial performance, patient satisfaction, and clinical focus while reducing system costs. Customers include independent urology practices, health systems, and ASCs requiring reliable access to stone management equipment with integrated technical and administrative support.

Natech Plastics is an ISO 13485- and ISO 9001-certified contract manufacturer specializing in custom injection molding and engineering services for medical devices, life sciences, and diagnostic consumables. Based in Ronkonkoma, New York, and founded in 1998, the company provides fully integrated solutions spanning product development, contract manufacturing, and packaging. Core capabilities include design for manufacturability, precision microstructure molding (down to 150nm features), cleanroom assembly, content filling with liquids and reagents, and custom software/IoT development. Natech serves medical device startups and established companies, supporting them from prototype through commercial production. The company operates state-of-the-art injection molding facilities (ARBURG equipment), maintains cleanroom manufacturing environments, and holds FDA 21 CFR 820 inspection status and ISO 15378 certification for primary packaging materials.

LPG America is the US subsidiary of LPG Group, a world leader in cellular stimulation and non-invasive treatment solutions. The company designs, distributes, and services endermologie® systems—patented mechanical massage devices used by healthcare professionals, aesthetic medicine practitioners, spas, and medical-spa facilities for body and facial treatments. Applications include medical indications (lymphatic drainage, scars, edema, burn rehabilitation) and aesthetic applications (cellulite reduction, body contouring, firmness, facial rejuvenation). Product portfolio includes the CELLU M6 Infinity®, CELLU M6 Alliance®, Mobi M6®, and Huber® 360. LPG America provides device sales, professional training, technical support, and annual servicing to 28,000+ equipped professionals worldwide.

Criticare Technologies, Inc. (CTI) is an international medical device manufacturer founded in 1984, headquartered in Warwick, Rhode Island. CTI specializes in patient monitoring devices and anesthetic gas monitoring systems designed for critical care, anesthesia, respiratory care, transport, and outpatient environments. The company's product portfolio combines technological innovation with cost-effective design to address patient safety and continuous monitoring requirements across acute and perioperative settings. CTI provides comprehensive technical support, equipment servicing, and rental-ownership programs to ensure affordability and consistent operational reliability for healthcare facilities.

Tritex Medical Manufacturing is a USA-based ISO 13485:2016–certified precision contract machining service provider specializing in the design and manufacture of surgical instruments and components. Located in Mount Morris, Michigan, the company has operated for over 30 years as an integrated supplier to medical device manufacturers, aerospace, defense, and transportation industries. Core manufacturing capabilities include CNC Swiss turning (Citizen machines, up to 32mm capacity), centerless grinding (Monza 300/400 equipment, 1–32mm diameter range), flute grinding and drilling for surgical drill bits and burs, laser cutting with pinpoint accuracy, laser engraving/marking for product identification, and bench-top finishing services including straightening and polishing. The company produces surgical drill bit blanks, saw blades, bur fluting, and custom-machined stainless steel components to tight tolerances. Tritex manufactures zero-defect components and emphasizes on-time delivery, competitive pricing, and quality assurance through a documented ISO 13485 Quality Management System. The facility is USA-based with state-of-the-art equipment and supports both high-volume production and short-run prototyping (including single-piece fabrication with quick turnaround). The company serves as a contract manufacturer for OEM medical device makers nationwide and internationally, providing supply-chain support for manufacturers requiring precision machining capacity, quality assurance, and regulatory compliance.

Vantage MedTech is a FDA-registered contract development and manufacturing organization (CDMO) specializing in complex electromechanical medical devices. Founded in 1994 with 30+ years of experience, the company employs over 150 specialized engineers across facilities in Kansas and New Jersey. Vantage MedTech provides end-to-end product lifecycle support including feasibility assessments, design and development, regulatory and clinical strategy, prototyping, manufacturing, and after-market services. The company has successfully developed over 1,600 medical devices for startups and established OEMs. Core expertise includes RF energy, microwave ablation, electroporation, medical device electronics, software/firmware design, human factors engineering, and validation/verification testing. Vantage MedTech leverages proprietary Advantage Platforms™ (AdvantagePFA™, AdvantageGFM™, AdvantageRF™, AdvantageUI™) to accelerate product development, reduce costs, and enable manufacturing scalability. ISO 13485 and multi-national regulatory certified.

Voltas Medical LLC is a vertically integrated medical device development and manufacturing partner headquartered in Cottage Grove, Minnesota. The company provides accelerated, end-to-end services for medical device commercialization under a single project manager, budget, and timeline. Core capabilities span R&D and rapid weekly prototyping (using Arduino, Raspberry Pi, sensors, LCD screens), regulatory services (510k submissions, PreSub/513g work), contract manufacturing (plastic injection molding, micro-molding, die-mold tooling), specialized processes (balloon development, hydrophilic/hydrophobic coatings, UV laser etching, RF and ultrasonic welding), in-house ETO sterilization with validation, packaging and blister tray development, and post-launch support including distribution, warehousing, medical sales, and marketing. The company targets Class I and Class II medical devices and claims capability to bring products to market in under 2 years for under $1 million. Device specialties include ablation catheters, stent delivery systems, diagnostic imaging, laparoscopic instruments, bone plates, endovascular grafts, neurostimulation devices, and vascular catheters.

The Sentinel Imaging Group is a full-service medical imaging distributor and service provider specializing in ultrasound systems, probes, and multimodal diagnostic imaging equipment. The company sells, services, and repairs diagnostic imaging equipment across ultrasound, CT, MRI, X-ray, and other imaging modalities. Primary product lines include ultrasound system sales (major brands: BK, GE, Philips, Mindray, Sonosite), ultrasound probe sales and repair, and comprehensive service packages including emergency on-site support, depot-level repairs, and preventive maintenance inspections. The company operates a state-of-the-art ultrasound probe repair laboratory offering free evaluations and fast turnaround. Service capabilities span multiple facility locations with multi-brand, multi-model support. The Sentinel Imaging Group markets to hospitals, surgery centers, diagnostic imaging practices, and sports medicine clinics. All equipment sold or repaired is covered by the Sentinel Advantage warranty. The company provides flexible financing options and emphasizes OEM-allegiant relationships to ensure quality and compatibility. Imaging consultants assist customers with probe selection and system compatibility verification.

Advantech Corporation is a global leader in embedded computing, industrial automation, edge AI, and intelligent healthcare solutions. The company manufactures industrial-grade computing platforms, edge AI systems, IoT devices, and healthcare-specific IT infrastructure. Product lines include embedded PCs, fanless computers, edge AI and GPU systems, industrial motherboards, medical computers and tablets, medical monitors, and operating room video solutions. Advantech also provides intelligent healthcare platforms (iHospital), medical carts and tablets, and comprehensive design-to-order manufacturing services. The company serves industrial, healthcare, retail, logistics, and transportation sectors with solutions for edge computing, data acquisition, automation control, and healthcare IT infrastructure. Advantech offers design and manufacturing services, global technical support, RMA services, training through IoT Academy, and a comprehensive eStore for procurement. The company emphasizes reliability, industrial-grade specifications, and integration with industry standards.

Coda Corp USA is a certified women-owned quality systems consulting firm specializing in pharmaceutical, biopharmaceutical, and medical device manufacturing. The company delivers comprehensive Quality and Operations Systems services, including quality systems consulting and assurance, process validation, Six Sigma and Lean project management, regulatory compliance remediation, and continual improvement initiatives. Coda focuses on CFR Title 21 compliance, process design, change control, root cause investigation, and GAMP Part 11 validation. The firm manages projects from local documentation efforts to global manufacturing system implementations, serving Fortune 500 companies through mid-market organizations. Coda emphasizes reducing process risk, ensuring cGMP compliance, and optimizing manufacturing excellence through expert guidance and collaborative partnership.

Emsere is a clinical trial solutions partner specializing in comprehensive equipment management, global logistics, and asset management services for pharmaceutical and biotechnology companies. Founded in 1995 and headquartered in Leiden, Netherlands, with an office in Zug, Switzerland, the company supports over 400 active clinical studies across more than 9,000 sites in over 100 countries. Emsere provides end-to-end equipment solutions including sourcing, rental, maintenance, and asset management of medical and laboratory devices. The company offers global logistics services covering equipment delivery, customs clearance, and on-site placement. Emsere's ATRIUM cloud portal provides integrated digital solutions for site management, budget tracking, and inventory oversight. Services include equipment installation, training, technical support, repairs, maintenance, end-of-life recycling, and ancillary supplies kit packing. With over 25 years of experience, Emsere positions itself as a true clinical trial partner rather than a transactional vendor, offering holistic support from study startup through completion.

Tii-Medical (Thorn Industries) is an ISO 13485-certified, vertically integrated medical device manufacturer specializing in precision CNC and additive manufacturing for surgical instruments and medical components. The company operates 7-axis Swiss machining (Tsugami), multi-axis CNC machining, and advanced 3D printing capabilities (Stratasys Polyjet J55 and FDM F370). With 22 years of experience, Tii-Medical provides end-to-end manufacturing solutions including reverse engineering, 3D scanning (Artec), design support (SolidWorks), heat treatment, passivation, and laser marking. Their vertically integrated approach enables in-house production from design through assembly, reducing lead times and costs. The company serves OEMs and medical device developers requiring high-precision components, surgical instruments, and proof-of-concept prototypes with full traceability and regulatory compliance.

RevZero, Inc. is a US-based precision medical device contract manufacturer specializing in regulated orthopedic implant manufacturing. Founded in 2007 and headquartered in Chanhassen, Minnesota, the company provides Design for Manufacturability (DFM) guidance, prototype development, and precision production services for medical device engineering teams. RevZero is ISO 13485:2016 certified and FDA-registered, supporting the full product development cycle from early design through production scale-up. The company manufactures complex orthopedic components including plates, screws, spacers, and assemblies for trauma and extremities applications; spinal devices such as interbody spacers, pedicle screws, rods, and fusion systems; and minimally invasive device components. Manufacturing capabilities include multi-axis CNC machining, Swiss turning, wire EDM, precision finishing, and laser marking. The company works with medical-grade materials including titanium, cobalt-chrome, stainless steels, and PEEK. RevZero emphasizes early manufacturing input to prevent late-stage revisions, predictable timelines, full inspection and traceability documentation, and direct engineer-to-engineer communication. The company positions itself as a partner that reduces revision cycles, improves design manufacturability, and delivers parts ready for real-world clinical use.

C2C Development, LLC is an FDA-registered, ISO 13485:2016-certified contract manufacturer and product development firm specializing in medical device design, prototyping, and low-volume manufacturing. The company operates a certified ISO 7 (Class 10,000) cleanroom environment and serves medical device innovators across laparoscopic, endoscopic, orthopedic, intravascular, neurological, stereotactic, and drug delivery applications. Services include comprehensive design control and prototyping using 3D modeling, 3D printing, conventional machining, and CNC machining; component sourcing and supplier qualification under ISO 13485 quality systems; assembly and packaging operations including kitting, cleaning, and inspection; verification and validation testing including packaging seal integrity, shelf-life, and mechanical/functional testing; sterilization management and laboratory testing coordination; and regulatory strategy consultation and submission support. The firm specializes in manual and semi-automated assembly for products that larger OEMs may not accommodate, enabling manufacturers to scale from pilot production to commercial release under either C2C's or the client's quality system. Clients include Medtronic, FHC, Monteris, and other established medical device manufacturers.

Paradyne Medical is a turnkey engineering and manufacturing solutions provider specializing in design, fabrication, and supply chain management for medical device and equipment manufacturers. The company serves both established OEMs and startups, offering comprehensive services including concept design and engineering, custom tooling and fixtures, manufacturing (including catheter and balloon fabrication, EPTFE sintering, ultrasonic welding, and RF welding), biocompatibility testing, product testing, quality control, and supply chain logistics. FDA-registered and procurement-certified, Paradyne Medical combines product development expertise with full-service manufacturing capabilities for the medical, biomedical, and life science industries.

Universal Diagnostic Solutions (UDS) is an FDA-registered distributor and service provider specializing in new and used portable ultrasound systems from major manufacturers including Mindray, GE, Philips, SonoSite, Chison, Siemens/Acuson, and others. Operating since 2004 from Vista, California, UDS provides comprehensive B2B support including equipment selection consultation, technical training, maintenance plans, repairs, and warranty services. The company serves diverse clinical applications including cardiology, obstetrics/gynecology, musculoskeletal imaging, anesthesiology, and pain management. UDS offers customizable ultrasound configurations with transducers, peripherals, and accessories tailored to specific practice requirements. The company maintains a 12,000 sq ft showroom with demonstration units and provides remote consultation, detailed product comparisons, and unbiased guidance for both entry-level and premium ultrasound systems.

Med One Group is a leading independent medical equipment leasing, rental, and sales company headquartered in Sandy, Utah, with nationwide operations since 1991. The company has completed over one billion dollars in lease transactions and operates distribution sites across California, Utah, Georgia, Colorado, Arizona, and Florida. Med One specializes in critical care medical equipment including infusion pumps (BD Alaris systems), ventilators, patient monitors, support surfaces, and hospital beds sourced from leading manufacturers such as BD, Baxter, and Hamilton. The company offers flexible acquisition solutions including capital leases, operating leases, equity rentals, deferred payments, and step-up payment arrangements tailored to hospital and acute care facility requirements. All equipment is delivered patient-ready and backed by comprehensive biomedical services including testing, maintenance, calibration, and the proprietary Asset Refresh Program. Med One's business model emphasizes transparency, competitive pricing, simple lease documentation without hidden fees, and responsive customer service to healthcare facilities nationwide.

PRO-TECH Design & Manufacturing is a contract manufacturing and outsourcing specialist serving the medical device industry for over 40 years. The company provides comprehensive end-to-end solutions including medical device contract packaging, contract assembly, custom sewn medical products, laboratory services, and sterilization services. Operating three full-scale manufacturing facilities in Santa Fe Springs, California; Arlington, Texas; and St. Paul, Minnesota, PRO-TECH serves clients ranging from Fortune 500 companies to emerging startups. The company holds FDA registration and ISO 13485 certification, with state-of-the-art Class 10,000/ISO 7-rated cleanroom facilities. Additionally, the company operates an ISO 17025-accredited laboratory providing packaging validation and testing services. PRO-TECH's service capabilities include custom design and prototyping, manual and automated sewing operations, contract packaging and assembly, sterilization services, and packaging validation testing. The company emphasizes quality assurance, customized solutions, responsive customer service, and long-term partnership development. Manufacturing expertise encompasses the full product lifecycle from design through market launch.

Diamond Diagnostics Inc. is a specialized clinical laboratory instrumentation and consumables supplier based in Holliston, Massachusetts, founded in 1996. The company manufactures, remanufactures, and supplies new and refurbished chemistry analyzers, electrolyte analyzers, immunoassay systems, blood gas analyzers, coagulation analyzers, hematology analyzers, and molecular analyzers. With approximately 80 employees and ~$19M annual revenue, Diamond offers over 500 consumable products including reagents, quality controls, and electrodes. The company's proprietary Down-To-Frame® refurbishment process restores equipment to like-new condition. Most products hold FDA clearance and CE approval. Diamond provides comprehensive field service, depot service, preventive maintenance, remote support, control assay, and refurbishment services to clinical laboratories and hospitals globally. ISO 9001:2015 and ISO 13485:2016 certified, the company also offers OEM and contract manufacturing for third-party organizations.

Block Imaging is a global leader in refurbished medical imaging equipment, parts, and multi-vendor service solutions. Founded in 1997 and headquartered in Holt, Michigan, the company employs over 300 team members across facilities in Michigan, California, France, and Japan. ISO-9001 certified and serving healthcare providers in over 100 countries, Block Imaging specializes in extending the operational life of diagnostic imaging systems across multiple modalities and vendors. The company offers a comprehensive ecosystem comprising 40,000+ validated imaging parts, flexible multi-vendor service with nationwide engineers, equipment sourcing and trading services, and rapid on-site support for U.S. customers. Block Imaging's Sourcing Window Pro platform enables centralized purchasing and inventory management. The company focuses on reducing equipment downtime, controlling costs, and maintaining performance consistency across aging and legacy imaging systems when original manufacturer support ends.

Pointcore is a healthcare services company providing nonclinical and back-end operational support to health systems. Primary service areas include Healthcare Technology Management (HTM) for medical equipment maintenance and servicing; Supply Chain Services focused on spend aggregation and cost reduction; Technology Services encompassing EHR (Epic) implementation, management, and optimization, plus IT and network infrastructure; Facilities Management and Construction Services; and Business Services for healthcare operations. The company offers proprietary consulting methodologies (PathSeeker Methodology™) and strategic partnership networks to deliver customized solutions. Pointcore serves health systems seeking to lower operational costs, overcome resource constraints, maintain technology currency, and ensure regulatory compliance. The company maintains healthcare-specific expertise in managing critical infrastructure and support systems that enable clinical delivery.

Criterion Precision Machining is a female-owned, ISO 9001 & ISO 13485 certified, FDA & ITAR registered precision machine shop specializing in tight-tolerance component manufacturing for medical devices, aerospace, defense, and photonics industries. The company manufactures prototype and production components for Class II & Class III medical devices, including surgical instruments, implants, and diagnostic instrumentation. Core capabilities include CNC milling, CNC turning, Swiss turning, and prototyping services. With AS9100 aerospace certification and DFARS compliance, Criterion supports design validation, proof-of-concept, clinical trials, and full-scale production. The company serves established partners including Riverpoint Medical, Smith & Nephew, and Corning, delivering components requiring ultra-tight tolerances, biocompatible materials, and FDA-compliant quality standards.

Planet Innovation is a full-service healthtech innovation, commercialization, and manufacturing company based in Victoria, Australia, with additional facilities in Irvine, California. Founded in 2009, the company employs over 300 experts delivering end-to-end contract development and manufacturing (CDMO) services across the product lifecycle. Certified to ISO 13485, Planet Innovation specializes in diagnostics, medical devices, biotechnology, and connected health solutions. The company provides comprehensive services including product design and engineering, commercialization strategy, digital health solutions, and contract manufacturing. Its market-pull approach leverages deep market insights to ensure products meet customer needs and achieve commercial success. Planet Innovation collaborates with leading global healthtech companies including Abbott, Merck, Quidel, Bio-Rad, and IDEX. The company has expanded capabilities through strategic acquisitions and partnerships, enhancing manufacturing capacity and expertise in digital health, patient monitoring, and emerging medtech areas.

PARAMETRIK is a medical device reprocessing services provider specializing in endoscope, surgical instrument, and robotic attachment reprocessing. The company operates FDA 510(k)-approved reprocessing facilities delivering PRECISE IFU (Instructions for Use) cleaning, detailed multi-point inspection, and terminal sterilization via ethylene oxide (EO) using validated systems. PARAMETRIK's proprietary MACH I Instrument Processor automates endoscope cleaning with protein removal validated to <1.2 µg/cm², eliminating the need for manual pre-cleaning on validated scopes and reducing operational costs by 50% or more. Off-site reprocessing services provide 24-hour turnaround with specialized facility transport, inspection, cleaning, and sterilization. The company addresses critical infection control gaps inherent in decades-old manual cleaning protocols, reducing patient risk, organizational liability, and staff training burden while supporting sustainable sterilization practices.