Surgical Instruments in Massachusetts

Tecomet, Inc. is a global precision contract manufacturer founded in 1963 and headquartered in Woburn, Massachusetts, serving the medical device, orthopedic, and minimally invasive surgical markets. With 2,000+ employees across 14 manufacturing campuses in five countries, Tecomet generates approximately $678.9 million in annual revenue. The company is recognized as the world's largest orthopedic contract manufacturer, delivering end-to-end manufacturing solutions from design prototyping through full-scale production. Tecomet specializes in complex, high-precision products utilizing proprietary technologies including photochemical etching, precision machining, additive manufacturing, net shape forging, casting, laser and electron beam welding, and robotic finishing. Core offerings include orthopedic implants (hip, knee, shoulder, spine, trauma & extremities), precision surgical instruments, minimally invasive surgical components, and specialized cases and trays. The company provides comprehensive services encompassing innovation and design consulting, rapid prototyping, packaging and sterile cleanroom assembly, and full production support. Its collaborative approach and rigorous quality standards make it a preferred partner for leading medical device OEMs seeking scalable, innovative manufacturing solutions for orthopedic and surgical device products.

Five Star Manufacturing, Inc. is an ISO 13485-certified, FDA-registered precision medical device manufacturer and surgical instrument repair specialist based in New Bedford, Massachusetts. The company operates two primary service lines: Five Star Manufacturing handles design and production of general hand-held surgical instruments, orthopedic instruments, implantable devices, and custom medical components from prototype through full-scale production. Five Star Surgical provides complete instrument lifecycle management, including factory-trained repair and restoration of surgical instruments to original manufacturer specifications. The company serves a dual customer base of original equipment manufacturers (including Zimmer Biomet, Arthrex, Smith + Nephew, DePuy Synthes, BD, and Integra) and healthcare systems (Northern Light Health, UMass Memorial, Boston Medical Center, Cambridge Health Alliance, Southcoast Hospitals Group). Manufacturing capabilities include precision machining, assembly, and quality control for instruments used in general surgery, orthopedic, and specialty procedures. Repair services encompass ultrasonic cleaning, instrument resharpening, functional testing, and restoration to meet or exceed industry standards. Five Star holds ISO 13485 medical device quality management certification, FDA device registration, and ITAR compliance (effective 2026). The organization emphasizes meticulous craftsmanship, attention to detail, and commitment to quality throughout manufacturing and repair processes. No specific product models or regulatory 510(k) clearances are detailed on the public website.

EDGe Surgical, Inc. manufactures the Electronic Depth Gauge (EDG), a precision surgical instrument designed to improve accuracy and safety in orthopedic plating procedures. The EDG is an electronic depth measurement device that determines correct screw length for plate-and-screw fixation, reducing the risk of implant waste, infection, and procedure complications. The company's core value proposition addresses documented clinical challenges: conventional depth gauges are difficult to sterilize, leading to contamination risk; they increase OR time through measurement errors and screw replacement; and they necessitate additional fluoroscopy exposure to staff and patients. The EDG is marketed as more accurate, universally compatible with all major orthopedic plating systems (DePuy Synthes, Smith & Nephew, Arthrex, Paragon 28, Zimmer Biomet Acumed, Skeletal Dynamics, Medartis, Stryker, Globus Medical, Trimed, Conventus, Flower), and designed to be cleanable and sterilizable. The company reports adoption in over 60 hospitals across the United States. EDGe Surgical positions its device as infection-control-focused and cost-effective, addressing both patient safety outcomes and procedural economics.

Tegra Medical is a global contract manufacturer specializing in end-to-end production of medical devices. Headquartered in Franklin, Massachusetts, with manufacturing facilities across the United States, Costa Rica, Switzerland, and Asia, the company employs over 1,000 people. Tegra Medical delivers comprehensive manufacturing solutions including design, prototyping, precision production, assembly, packaging, and sterilization for complex metal and plastic components. The company serves multiple therapeutic areas including oncology, orthopedics, cardiology, minimally invasive surgery, ophthalmic, women's health, drug delivery, and robotic-assisted surgery applications. Advanced manufacturing capabilities include Swiss machining, multi-axis milling, injection molding, wire grinding, and precision finishing. Tegra Medical maintains ISO 13485 certification and FDA registration, supported by rigorous quality management systems. The company also operates Quick Wire & Tubing, an e-commerce platform offering in-stock and custom wire, tubing, and secondary processing services for medical device development and prototyping.

Boston BGEcare Inc. is a Massachusetts-based medical consumables and contract manufacturing company specializing in wound care, personal protective equipment (PPE), compression garments, ostomy products, advanced wound care solutions, and operating room/surgical supplies. The company operates as both a direct product supplier and an original equipment manufacturer (OEM) partner, offering turn-key contract manufacturing services from product ideation through commercialization. BGEcare serves healthcare providers and manufacturers requiring transparent, efficient, and resilient supply chain solutions. The company maintains quality and regulatory compliance capabilities as core operational competencies, supporting FDA and other regulatory pathways. Product lines span traditional wound care (gauze, bandages, dressings), compression therapy systems, ostomy accessories, advanced wound management technologies, and surgical/OR consumables. BGEcare positions itself as a manufacturing partner for companies seeking to develop, scale, or outsource production of medical devices and consumables, emphasizing operational transparency and supply chain resilience.

Hood Laboratories, founded in 1962, manufactures specialized medical devices for head, neck, and chest surgery with focus on airway management and otolaryngology. The company originated as the original manufacturer of T-Tubes for otolaryngologists and has expanded to serve rhinologists, allergists, laryngologists, speech-language pathologists, and thoracic surgeons. Core product lines include laryngeal stents (Mehta stents), tracheal-bronchial stents (Harrell Y-Stents), salivary management devices (Schaitkin Salivary Duct Cannula and Walvekar Salivary Duct Stents), and rigid bronchoscope systems (Efer bronchoscopes). Products are used at leading medical centers including Beth Israel Deaconess Medical Center. Hood maintains emphasis on quality control, custom manufacturing capabilities, and collaborative product development with clinical specialists. The company operates as a niche medical device manufacturer with established relationships in interventional pulmonology and surgical specialty markets.

SchureMed is a medical equipment manufacturer specializing in surgical patient positioning equipment for orthopedic, gynecological, urological, laparoscopic, and pediatric procedures. The company designs and manufactures in-house a comprehensive line of operating room positioning devices, including surgical table accessories, positioning pads, stirrups, surgical beach chairs, and custom OEM solutions. Key products include the SchureLoc XPS, Great White Platinum Stirrups, E-Z Lift Surgical Beach Chair, and TKR Positioner. SchureMed emphasizes collaboration with surgeons and OR staff to develop tailored positioning solutions that enhance patient safety, comfort, and surgical access while minimizing pressure points. All products are manufactured in the USA, ISO 13485:2016 certified, and distributed globally.

Ranfac Corp. is an ISO 13485:2016-certified Contract Development and Manufacturing Organization (CDMO), Original Equipment Manufacturer (OEM), and Contract Manufacturing Organization (CMO) specializing in custom Class I and Class II single-use hypodermic-based medical devices. Founded in 1888 and based in Avon, Massachusetts, Ranfac operates a vertically integrated 40,000 sq ft facility that manages all production stages in-house: metal machining (12 specialized processes including CNC, laser welding, electropolishing), polymer injection and insert molding (Class 8 cleanroom), cleaning and passivation, cleanroom assembly (Class 7 ISO), and EO sterilization via exclusive STERIS partnership. The company serves minimally invasive surgery access devices, biopsy and aspiration systems, orthobiologics delivery cannulas, interventional radiology components, hematology devices, and general surgery instruments. Ranfac supports low minimum order quantities and scales from prototype to 500K+ units annually. MDSAP, EU MDR, and FDA registered, enabling simultaneous access to seven export markets.

Microline Surgical manufactures reposable surgical instruments designed to reduce total cost of ownership and environmental impact while maintaining surgical precision and safety. The company specializes in laparoscopic and electrosurgical instrument platforms that enable healthcare facilities to balance quality instrument performance with cost efficiency. Their reposable instrument approach replaces traditional single-use disposables, allowing surgeons access to precision instruments with new tips while reducing waste and facility expenses. The company serves operating rooms and surgical centers, with particular emphasis on minimally invasive procedures. Microline's solutions are positioned for healthcare professionals seeking sustainable, cost-effective surgical instrument management without compromising clinical outcomes. The company has demonstrated market expansion through strategic acquisitions, including surgical instrumentation assets from Retraction Limited (2023), indicating growth in their surgical instrument portfolio.

Amsel Medical Corporation develops minimally invasive surgical occlusion devices for vessel and tubular structure closure. The company's primary product, SCureClamp™ with Interdigitation Occlusion Technology (iDOT™), is a mechanical surgical clamping device FDA-cleared and CE-marked for closing blood vessels, arteries, veins, and ducts during surgical and interventional procedures. The device employs a unique transfixing mechanism delivered through an 18-gauge needle, providing permanent, non-chemical, non-thermal occlusion similar to hand-sewn transfixion sutures. Key design features include anchoring technology to prevent slippage, accommodation of vessels 2.0–7.0 mm in diameter, and ultrasound-guided deployment. Amsel's SCureClamp targets multiple surgical specialties including vascular surgery, general surgery (bariatric, cardiac, oncology), trauma management, and interventional radiology. In vascular applications, the device addresses limitations of current perforator treatments (lasers, RF, glue, sclerotherapy), which average 75–80% efficacy and lack permanent solutions. Clinical evidence from peer-reviewed publications in the Journal of Vascular Surgery, Surgical Endoscopy, and Journal of Surgical Research demonstrates preclinical efficacy in porcine models. The company is also developing a temporary clamping variant for military trauma applications, specifically targeting non-compressible and junctional hemorrhage in prehospital environments. Amsel Medical was awarded a prestigious U.S. Air Force AFWERX Phase 2 SBIR grant for this development. The company's devices are indicated for use by vein physicians, general surgeons, vascular surgeons, cardiovascular surgeons, interventional radiologists, and military medical personnel. Manufacturing and regulatory compliance align with FDA 510(k) and CE Mark standards.

D&R Products is a contract manufacturer of medical devices headquartered in Hudson, Massachusetts, with over 80 years of continuous American manufacturing and 38 years of specialized focus on medical device outsourcing. The company operates a 43,000 square-foot facility providing turnkey manufacturing from bar stock to finished device. D&R holds ISO 13485-2016 certification and maintains in-house control over key manufacturing processes including CNC machining (Swiss turning, wire EDM), secondary operations (deburring, electropolishing, passivation, laser marking), precision welding (laser, palm arc, resistance), and clean room assembly (ISO Class 7 and 8). The company specializes in exotic materials including nitinol, titanium, stainless steel, and engineered polymers (PEAK, Radel). Product specialties include minimally invasive surgical devices, arthroscopic shaver blades and burrs, RF electrodes, soft tissue refixation implants, specialty needles, cannulas, and trocars. D&R maintains direct executive and engineering engagement for each customer project, offering design-for-manufacturability consultation and custom process development. The company reports being a sole-source supplier on over 75% of products and counts 6 of the 7 largest medical device companies among its customer base. Manufacturing capabilities span small lots through millions of units with documented traceability and quality system control.

Beeken Biomedical is a medical device company specializing in hemostatic wound care and bleeding control products. The company develops, licenses, and commercializes advanced surgical dressings and trauma care solutions under the NuStat® brand. The flagship product line is built on proprietary Hemafiber™ technology—a hemostatic fiber matrix that accelerates clot formation through absorption and local concentration of clotting factors at the wound site. NuStat® products are FDA Class II cleared for temporary control of internal organ space bleeding in class III and IV hemorrhage cases, as well as for severely bleeding wounds including surgical and traumatic injuries. The company serves multiple markets: hospital surgical and trauma departments, first responders (military, law enforcement, fire, and EMS), and public/private safety facilities. NuStat® OTC products meet or exceed U.S. Department of Defense specifications for quality and functionality and align with Stop the Bleed® initiatives. Beeken Biomedical holds FDA 510(k) clearance and maintains product compliance with relevant medical device regulations. The company combines B2B hospital/surgical supply channels with direct-to-consumer and public safety distribution.

AliMed, LLC is a medical supplies manufacturer and distributor based in Dedham, Massachusetts, with over 50 years of industry experience since 1970. The company specializes in innovative healthcare products including durable medical equipment, rehabilitation aids, operating room accessories, and ergonomic solutions. AliMed's core product portfolio encompasses patient positioning systems (AliBlue™ Gel and AliBlue™ Lite hybrid gel-foam positioners), surgical positioning straps and supports, orthopedic footwear and insoles, wheelchair cushions, hand and wrist braces, lower extremity positioning aids, and therapy equipment. The company serves hospitals, ambulatory surgery centers, post-acute care facilities, and home care settings. AliMed is recognized for customization capabilities, responsive U.S.-based customer service, same-day shipping on in-stock orders, and volume pricing. The company was named Manufacturer of the Year by the Massachusetts Legislative Caucus.

Advamedica Inc. is a deep science medtech company specializing in novel biomaterial-based medical devices. The company leverages proprietary biomaterial technology and manufacturing platforms to develop innovative hemostatic, surgical, and wound care products for pre-hospital, intra-operative, and post-operative clinical settings. Their product portfolio includes FDA-cleared hemostatic patches and surgical hemostats based on chitosan and protonated bioadhesive technology, as well as advanced wound care dressings. Advamedica's solutions are designed to improve patient outcomes through strong bioadhesion, ease of removal, and barrier properties against bacterial penetration, with products available in 40+ countries.

A.M.I. (Agency for Medical Innovations GmbH) is an Austrian medical device manufacturer specializing in innovative surgical solutions for Coloproctology, Urology, and Urogynecology. The company develops and manufactures minimally invasive surgical instruments and implantable devices designed to reduce patient pain, discomfort, and surgical complications while enhancing treatment outcomes. Primary product lines include the HAL-RAR system for hemorrhoid treatment, the ATOMS artificial urinary sphincter for stress urinary incontinence, incontinence slings (TVA/TOA) with post-operative adjustability, pelvic floor reconstruction meshes (HexaPro, BSC, inGYNious, CR-Mesh), the Soft Anal Band for fecal continence restoration, and the i-Stitch instrument for minimally invasive prolapse fixation. The company collaborates with internationally recognized surgeons and experts to ensure clinical validation and product refinement. A.M.I. markets its products globally to hospitals and surgical centers, with particular strength in European markets. The company maintains quality and safety standards through international certification and regulatory compliance. Manufacturing and distribution operations are based in Feldkirch, Austria.

American Surgical Company is a U.S.-based innovator specializing in single-use neurosurgical instruments and surgical consumables manufactured with 100% wind-powered electricity. The company focuses on precision disposable tools designed for microsurgery, minimally invasive procedures, and complex cranial operations. Its product portfolio includes neurosurgical patties (DeliCot®, Ray-Cot®, Uniqcot™, Telfa®, Americot®, and tapered variants) engineered for optimal tissue protection and brain retraction with minimal trauma. Additional offerings include the ATLAS™ Choice Disposable Non-Stick Bipolar Forceps for precise coagulation with reduced thermal damage, RhinoStop™ nasal packing for hemostasis management, ComfortPack™ eye pledgets for ophthalmic procedures, and X-ray detectable cotton balls. With over 35 years of market presence, 98% customer retention, and endorsements from leading neurosurgeons and academic institutions, ASC serves over 70 countries across six continents. The company actively supports the neurosurgical community through educational initiatives, case studies, and professional engagements.

Path Scientific, LLC is a privately held medical device company specializing in minimally invasive smart drilling systems. The company's flagship product, PathFormer, is a precision nail drill device that creates microconduits in finger nails and toenails to enhance drug delivery for treating onychomycosis (nail fungus infection) and providing pain relief from subungual hematoma (black toe). The procedure is quick (approximately 5 seconds per microconduit), painless, and safe, with automatic microcutter retraction. Path Scientific also develops transdermal products that create pathways in skin and nail for drug delivery, analyte extraction, fluid drainage, and ECG measurement improvement. Additionally, the company manufactures programmable orthopedic drilling devices capable of drilling precise bone holes at surgeon-specified or automatic depths, with control over penetration beyond the far cortex. All products emphasize minimally invasive, user-friendly design for clinical efficacy.

OrthoFundamentals, LLC (now operating as Demetra Spine following acquisition by Demetra) designs and manufactures single-use surgical kits and 3D-printed implants for orthopedic and spinal surgery, with specific focus on SI (sacroiliac) joint fusion procedures in the outpatient surgery center market. The company's core platform combines pre-sterilized, single-use instrument trays with sterile-packed 3D-printed implants and RFID-enabled inventory management and automatic billing systems. Products are designed to eliminate contamination risk, instrument delays, and case cancellations caused by damaged packaging or missing instruments—key pain points in ambulatory surgery centers (ASCs). The Trellis SI Joint Fusion System represents the company's flagship offering. OrthoFundamentals targets orthopedic surgeons and ASC operators seeking cost-efficient, high-quality alternatives to traditional hospital-based care models. The company emphasizes value-based solutions and accessibility for outpatient settings, positioning itself against the complexity and cost of legacy MedTech commercial models. Manufacturing capabilities include 3D printing of implants and assembly of sterile procedural kits. The company holds regulatory clearance sufficient to market spinal fusion implants and surgical instruments in the US market, though specific 510(k) or FDA clearance details are not specified on the website.

Cunningham Woodland Inc. is a New England-based medical distributor and repair specialist serving hospitals and surgical facilities for over 45 years. The company specializes in surgical instruments, sterilization equipment, and comprehensive repair services for operating rooms and sterile processing departments. As an ISO 13485:2016-certified facility, CWI provides surgical instrument repair with technicians averaging over 10 years of experience, mobile repair labs, in-hospital repair shops, and sterilizer cleaning services. The company also distributes single-use surgical consumables and offers repair tracking technology to streamline customer operations. Operating as a member of the Alliance of Surgical Distributors (ASD), CWI combines regional expertise with specialized clinical support across New England and beyond.

Jarvis Surgical, Inc. is a fifth-generation, privately held orthopedic manufacturing company with roots tracing to 1901 and formal incorporation in 1993. The company specializes in precision components and finished orthopedic devices for the surgical market. Product portfolio encompasses foot/ankle, knee, hip, spine, and shoulder implants and instruments. The company emphasizes lean manufacturing processes, customer service, and engineering capabilities. Based in Westfield, Massachusetts, Jarvis Surgical operates as a contract manufacturer and supplier to orthopedic device companies and surgical facilities. The company maintains FDA compliance and quality standards appropriate to implantable medical device manufacturing, though specific regulatory certifications (510(k), ISO 13485) are not detailed on the website. Manufacturing and design capabilities support custom and standard orthopedic implant solutions across multiple anatomical sites.

Viant Medical is a vertically integrated contract manufacturing partner specializing in medical device design, development, and full-scale production. The company operates 25 global locations with 2.3 million square feet of factory space, including 299,000+ square feet of ISO-certified clean room capacity. Viant serves OEMs across multiple clinical markets: orthopedics (instruments, implants, delivery systems, UHMWPE components), surgical technologies (minimally invasive surgery, robotics, endoscopy, ophthalmology, wound care, biopsy, aesthetic surgery), cardiac and interventional devices (overmolding, nitinol tubing, hypotube precision components), drug delivery (auto-injectors, IV sets, connectors, respiratory devices), bioprocessing (containment, transfer, filtration systems), bioelectronics (pain management, sleep apnea, wearables), diagnostics and laboratory products (injection tubes, chromatography tubing), and respiratory/monitoring/patient care (masks, trach tubes, airway tubes, console components). Core manufacturing capabilities include precision metals and metal tubing, medical-grade plastics and silicone molding, extrusions, tooling, automation, device assembly, and finished device services. The company provides end-to-end solutions from prototyping through sterilization and packaging management. Viant emphasizes vertical integration to ensure quality control, reduce supply chain risk, and accelerate time-to-market. The ViaLaunch™ program offers program management support. The company focuses exclusively on medical device manufacturing and maintains operational expertise in complex assembly, overmolding, and materials science.

PHASE(n) is a Boston-based contract manufacturing and product development partner specializing in medical device design, process optimization, and second-source manufacturing. The firm provides extended R&D capability to medical device OEMs, supporting projects from concept through manufacturing scale-up. Core competencies include new product design, prototype development, process improvement, quality engineering, and cleanroom assembly. PHASE(n) has documented experience with RF electrodes, powered arthroscopic instruments, and sterile single-use and reusable medical accessories. The company emphasizes collaborative partnerships, cost containment, quality assurance, and accelerated scaling for growing medical device businesses. Services are structured to augment in-house R&D teams without requiring full-time headcount additions.

Global Interconnect, Inc. (Gii) is a contract manufacturing partner specializing in custom connectors, cable assemblies, and electromechanical components for energy-based and diagnostic medical devices. Established in 1995 and ISO 13485/ISO 9001 certified, Gii serves leading medical device OEMs with custom engineering, design optimization, and precision manufacturing of performance-critical sub-assemblies and finished devices. The company operates manufacturing facilities in Massachusetts, Florida, and China, emphasizing value engineering, regulatory compliance, and supply chain efficiency. Gii's expertise spans surgical instrumentation, diagnostic imaging devices, ablation systems, endoscopy equipment, and specialty medical instrumentation. Their service model combines advanced manufacturing capabilities with engineering consultation to accelerate product development, reduce costs, and ensure quality and safety standards for MedTech OEMs globally.

TISSIUM is a medical device company founded in 2013 that develops biomorphic programmable polymers for tissue reconstruction and repair. The company's proprietary technology platform consists of biocompatible polymer building blocks that can be customized to match tissue-specific requirements while conforming to and integrating with surrounding tissue. TISSIUM currently markets COAPTIUM® CONNECT, the first and only FDA-authorized system for atraumatic sutureless nerve coaptation in peripheral nerve repair, which is commercially available in the United States. The company has received FDA De Novo clearance for its lead product and has completed two clinical studies, with 10 peer-reviewed publications and 26 patent families filed (88 patents granted). TISSIUM's pipeline extends across multiple therapeutic areas including peripheral nerve, cardiovascular, and gastrointestinal applications, with both open surgical and minimally invasive procedure formats. The company operates as a medical device manufacturer with focus on surgical reconstruction solutions for patients with damaged or injured tissue. Regulatory credentials include FDA De Novo authorization and adherence to medical device manufacturing standards.

TESco Associates, Inc. is a specialized contract manufacturer and research & development partner for bioabsorbable medical devices and implants. Founded in 1980 and headquartered in Tyngsborough, Massachusetts, the company operates a 15,000 sq. ft. cGMP-compliant facility with 12 Class 10,000 cleanroom suites. TESco provides comprehensive services across the medical device lifecycle: product development support, material selection and custom polymer formulation, mold design and fabrication, and manufacturing problem-solving from concept through clinical trials and commercial production. The company has developed proprietary polymer processing techniques for injection molding, extrusion, and specialty material blending, with expertise in low molecular weight loss and residual monomer control. TESco's portfolio includes bioabsorbable orthopedic implants, surgical screws, plates, clips, and interference devices. The firm serves as an outsourced partner for medical device companies requiring specialized expertise in bioabsorbable polymeric systems and has supported development of hundreds of bioabsorbable products.