Endoscopic Surgery Tools

186 vendors serving US medical buyers

Browse vendors of endoscopic surgery tools (Minimally Invasive Surgery) serving hospitals, clinics, laboratories, and other medical buyers across the United States. MedIndexer connects procurement and clinical-engineering teams with verified vendors supplying endoscopic surgery tools. Browse detailed profiles, compare service areas, and contact vendors directly — free for buyers.

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da yu enter prise co.,ltd.

Total Vein Systems is a medical device and consumables supplier specializing in vein surgery and interventional vascular procedures. Founded in 2003, the company markets an extensive product line of over 372 items including laser fibers, venous access devices, procedure packs, microphlebectomy instruments, compression hosiery, and surgical supplies. The TVS 1470 is their flagship open laser system featuring fibers with standard SMA connectors, designed for endovenous laser ablation and related minimally invasive vascular procedures. The company manufactures infiltration tubing kits and pump delivery systems with high-flow, large-bore configurations for rapid sterile solution delivery. All products are manufactured under ISO 13485 and KEMA standards, demonstrating commitment to medical device quality and regulatory compliance. Total Vein Systems emphasizes competitive pricing and customer service, positioning itself as a comprehensive single-source supplier for vein procedure requirements across clinical settings. The product portfolio addresses both procedural consumables and durable equipment needs for vascular surgery programs.

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Medfix International, LLC

Medfix International, LLC manufactures and distributes specialized surgical instruments for spinal, orthopedic, and minimally invasive procedures. Based in Tucson, Arizona, the company offers an extensive catalog of retractors, rongeurs, curettes, elevators, dissectors, forceps, scissors, needle holders, and ancillary surgical tools used in cervical, thoracic, and lumbar spine surgery, as well as general orthopedic applications. Product lines include the Medfix® VISION series of retractor systems designed for minimally invasive spine (MIS) and tubular procedures in various sizes (18mm, 22mm, 26mm), single-use Kerrison rongeurs, lumbar and cervical curette sets, disc preparation instruments, and spinal distraction systems. The company also manufactures specialized instruments for screw removal, pedicle probing, rod bending, and implant removal. Additional offerings include suction tubes, cast removal equipment, mallets, tamps, and bone-cutting instruments. Medfix serves orthopedic and neurosurgical facilities across the USA and Mexico. The company provides direct sales support through a dedicated team and maintains detailed product catalogs organized by instrument type. All instruments are manufactured to support both open and minimally invasive surgical techniques, with particular emphasis on spine surgery applications.

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LINA MEDICAL APS

LiNA Medical ApS is a minimally invasive gynecology device manufacturer headquartered in Denmark with North American operations in Norcross, Georgia. The company develops and markets single-use and cordless surgical instruments for hysteroscopic and laparoscopic procedures. Core product lines include the LiNA OperåScope (single-use operative hysteroscopy system), LiNA Librata (cordless endometrial ablation device), LiNA Xcise (cordless laparoscopic morcellator with morcellation bag), LiNA Loop (monopolar and bipolar loops for laparoscopic supracervical hysterectomy), and UroCure Arc Sling System (transvaginal sling for urology). Ancillary products include LiNA SeaStar (elastic retraction system), LiNA LapGuard (laparoscopic smoke filtration), LiNA McCartney Tube (transvaginal tube), and LiNA Versascope (single-use sheath for operative hysteroscopy). The company emphasizes simplified, innovative technology to reduce capital costs and procedural complexity while improving patient outcomes. LiNA Medical actively participates in major gynecology and urology society conferences including AAGL, ESGE, ACOG, AUA, and ASRM. The company provides both traditional purchase order fulfillment and online ordering through their webstore, with US customer service available Monday–Friday, 9:00 AM–5:00 PM ET.

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STRYKER CORP.

Stryker Corporation is a global medical technology company headquartered in Portage, Michigan, serving hospitals, surgical centers, and healthcare providers worldwide. The company manufactures and distributes a comprehensive portfolio of medical devices, surgical equipment, implants, and visualization systems across multiple specialties including orthopedics, neurosurgery, spine, trauma, cardiovascular, endoscopy, acute care, and emergency medicine. Key product categories include joint replacement implants (hips, knees) with Mako Robotic-Arm Assisted Technology, neurosurgical and spine instruments with 3D-printed technologies, minimally invasive surgical systems (laparoscopy, arthroscopy, endoscopy), emergency care equipment, communications systems for patient environments, interventional spine products (vertebroplasty, radiofrequency ablation), craniomaxillofacial solutions, sports medicine implants, and neurovascular stroke care devices. Stryker operates manufacturing facilities in multiple countries including Canada, China, and the US. The company maintains a strong commitment to sustainability through device reprocessing and remanufacturing services for single-use medical devices. With regional headquarters and distribution centers across the Americas, Europe, Asia-Pacific, and Middle East & Africa, Stryker provides integrated sales, service, and technical support. The company is regulated by the FDA and maintains global certifications for medical device manufacturing and quality management systems.

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Integra LifeSciences Corporation

Integra LifeSciences Corporation is a global medical technology company specializing in surgical, neurologic, and regenerative care products. The company manufactures and distributes a comprehensive portfolio spanning neurosurgery (dural repair, cranial reconstruction, hydrocephalus management, CSF drainage systems, multimodal neuro-critical care monitoring), wound reconstruction and care (engineered collagen, fetal bovine dermis, urinary bladder matrix, amniotic tissue, Manuka honey dressings, total contact casting), surgical reconstruction (nerve and tendon repair, hernia repair, plastic and reconstructive surgery), surgical instrumentation and lighting (including brands Jarit®, MicroFrance®, Omni-Tract®, Ruggles®-Redmond™, Padgett®, and Miltex®), and ear, nose and throat devices (airway dilation systems, balloon sinuplasty, nasal dilation, Eustachian tube dilation, navigation systems). The company serves hospitals, surgery centers, and tissue banks globally. Integra maintains extensive international operations with customer service, repair, and medical inquiry support across North America, Europe, Asia-Pacific, and other regions. The company provides clinical documentation, IFUs (Instructions for Use), and regulatory support resources on its products portal.

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Confluent Medical Technologies, Inc.

Confluent Medical Technologies is a contract manufacturer specializing in design, development, and large-scale manufacturing of interventional catheter-based devices and implants. The company manufactures over 492,931 components annually across 400,000+ square feet of production capacity with 987+ employees and 98+ engineers. Core capabilities include precision Nitinol (nickel-titanium) components and tubing, high-precision polymer tubing (PTFE and polyimide), complex and balloon catheter systems, biomedical textiles (wovens, knits, braids, non-wovens, and electrospun materials), catheter components (sheaths, dilators), and polymer stent coverings. Products include Filmcast PTFE tubing (mandrel sizes 0.010"-0.137", wall thickness 0.0005"-0.002", 3-4 week lead times) and the recently launched Filmcast Select™ and Ultra Polyimide formulations for tailored performance. The company provides rapid prototyping, laser cutting and welding, design consultation, and testing services. Serves interventional cardiology, endovascular surgery, and other catheter-based device markets. Operates manufacturing facilities in Scottsdale AZ, Fremont CA, Orange County CA, Warwick RI, Windham ME, Austin TX, Chattanooga TN, and internationally in Costa Rica and India. Regulatory credentials and specific certifications not explicitly stated on provided content.

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Medyssey USA

Medyssey USA, Inc. is the U.S. division of Medyssey, a medical device company founded in 2003, headquartered in Temecula, California. The company specializes in developing and commercializing orthopedic and neurosurgical spinal implants, with a focus on motion preservation and dynamic stabilization technologies. Medyssey's product portfolio includes spinal implants and systems designed for minimally invasive surgery, deformity correction, and posterior lumbar interbody fusion. The company has achieved multiple US-FDA 510(k) clearances and Health Canada licenses. With a strong research and development pipeline and presence in over 30 countries across six continents, Medyssey is committed to advancing spinal surgery outcomes through innovative implant technologies, including proprietary features such as linear slot compression mechanisms and dove-tail joint designs that enhance surgical stability and reduce complications.

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NUMED, INC.

NuMED, Inc. is a 35+ year established manufacturer of innovative cardiovascular medical devices specializing in minimally invasive interventional solutions for congenital heart defects and peripheral vascular disease. The company manufactures over 26 interventional brands distributed across more than 100 countries globally. NuMED's comprehensive product portfolio focuses on pediatric interventional cardiology, including advanced balloon catheter systems, stent technologies, and catheterization lab equipment designed for diagnostic and therapeutic procedures. The company is committed to collaborating with global thought leaders and interventionalists to develop high-quality, clinically superior devices that improve patient outcomes in congenital heart treatment. With a strong presence in the international interventional community and founding sponsorship of PICS (Pediatric Interventional Cardiology Society) since 1997, NuMED combines decades of manufacturing expertise with ongoing innovation in catheter design, stent delivery systems, and hemodynamic interventional tools.

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Iridex Corporation

Iridex Corporation is a medical technology company established in 1989, specializing in laser-based medical systems and devices for ophthalmology and select ENT applications. Headquartered in Mountain View, California, Iridex is recognized as a global leader in ophthalmic laser technology. The company offers a comprehensive portfolio of laser systems, delivery devices, retinal surgical instruments, consumables, and glaucoma devices. Flagship products include the PASCAL® laser system with patented MicroPulse™ technology, Cyclo G6, OcuLight, IQ 532, IQ 577, G-Probe systems, and MicroPulse P3 devices for transscleral cyclophotocoagulation. Iridex's MicroPulse® technology enables safer, tissue-sparing treatments for retinal diseases including diabetic macular edema, age-related macular degeneration, and central serous chorioretinopathy, as well as non-incisional glaucoma management. The company distributes directly in the U.S. through a sales force and via approximately 60 independent distributors across over 100 countries. Iridex provides extensive physician education, clinical support, training, and humanitarian initiatives.

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Pediatric Medical Device Marketing And Distribution LLC

Pediatric Medical Device Marketing and Distribution LLC is a specialized B2B distributor of pediatric medical devices, with a primary focus on minimally invasive surgical solutions for chest wall deformity correction. The company distributes state-of-the-art technologies designed to enhance patient outcomes in pediatric surgical settings. Their flagship product line is Park's Pectus System, a preferred toolkit for surgeons performing minimally invasive procedures to correct pectus deformities in pediatric patients. The system includes both surgical instruments and implantable devices (curved metal bars) that provide a less invasive alternative to traditional open surgical approaches, enabling gradual chest wall reshaping with improved recovery profiles. The company serves hospitals, operating theaters, and surgical centers, providing comprehensive ordering and technical support to healthcare organizations.

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Q3 Medical USA, LLC

Q3 Medical USA, LLC is a subsidiary of Q3 Medical Group, an Irish medical device holding company specializing in the development, manufacturing, and global distribution of innovative minimally invasive and biodegradable medical devices. The company focuses on cardiology, peripheral vascular, and non-vascular applications, with particular expertise in biodegradable implants, micro-invasive technologies, and drug delivery platforms. Q3 Medical's flagship product, ARCHIMEDES, is the first fully biodegradable biliary and pancreatic stent, designed to eliminate the need for removal procedures while reducing complications and healthcare costs. Operating through subsidiaries in Germany, China, and the USA, the company employs a clinician-led, multidisciplinary approach to develop patient-centric solutions that streamline treatment pathways, reduce hospital stays, and lower overall healthcare expenses. The company is committed to advancing sustainable healthcare through innovative technologies that balance superior patient outcomes with economic and environmental benefits.

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HJY Smart Medical Device Co., Ltd.

HJY Smart Medical Device Co., Ltd. (HJY Forward Medical Investment) is a Taiwan-based medical device manufacturer specializing in minimally invasive endoscopic surgery solutions and AI-assisted surgical technologies. Established in 2019, the company develops and manufactures innovative endoscopic vision systems addressing unmet needs in neuro- and orthopedic surgery. HJY's product portfolio includes FDA-approved VisualNext® 2D endoscopic vision systems for diagnostic and surgical applications, next-generation 3D head-mounted display (HMD) technology for real-time surgical visualization, and the HJY-YESS posterior lumbar retractor system for spine surgery. The company operates subsidiaries across China and the USA, positioning itself as a leader in next-generation endoscopy medtech with a focus on AI-integrated surgical platforms. HJY combines hardware innovation with artificial intelligence to advance minimally invasive surgical techniques.

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Fesarius Therapeutics

Fesarius Therapeutics is a bioregenerative surgical company specializing in advanced dermal tissue regeneration solutions. The company develops innovative hydrogel-based scaffold technology for treating full-thickness skin loss resulting from burns, trauma, plastic surgery, and tumor removal. Fesarius's flagship product, DermiSphere™ hDRT, is a dual-density collagen hydrogel dermal regeneration template featuring a unique microarchitecture that supports rapid cellular invasion and vascularization. The template maintains ideal wound bed conditions while facilitating stable tissue regeneration, achieving 100% wound bed incorporation by Day 3 and full vascularization by Day 7 in pre-clinical studies. Designed for ease of clinical use with omnidirectional application, conformability to irregular wound topographies, and in-situ trimming capability, DermiSphere addresses the unmet need for effective dermal reconstruction in wound care and reconstructive surgery applications.

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Airiver Medical

Airiver Medical is a clinical-stage medical device company developing minimally invasive technologies for the treatment of respiratory tract conditions. The company's lead product candidate is a Drug Coated Balloon platform targeting two primary indications: central airway stenosis (including subglottic, tracheal, and bronchial stenosis) and chronic rhinosinusitis (CRS). Central airway stenosis is a common complication following lung transplantation, prolonged intubation, and tracheostomy, affecting 7–18% of post-transplant patients. CRS is one of the most prevalent chronic conditions globally, affecting approximately 39+ million people in the U.S., with approximately half requiring surgical intervention. Airiver's Drug Coated Balloon is designed to provide sustained airway patency and potentially reduce the need for repeat procedures. The company has secured FDA Investigational Device Exemption (IDE) approval for pivotal clinical trials in both indications and is led by experienced medtech executives with backgrounds at Boston Scientific, Lutonix, Entellus Medical, and other leading device manufacturers.

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Aspero Medical, Inc.

Aspero Medical is a Boulder, Colorado-based medical device manufacturer specializing in innovative endoscopy technology for gastrointestinal (GI) procedures. Founded in 2018, the company develops patented balloon overtube systems designed to enhance diagnostic and interventional GI endoscopy. Their flagship Pillar™ technology features micro-textured balloon surfaces that improve mucosal wall traction and anchoring consistency in the GI tract, enabling deeper scope advancement and reducing procedure time. The Ancora-SB small bowel balloon overtube received FDA clearance in 2023. Aspero Medical's solutions address technical challenges in balloon endoscopy for small bowel disease diagnosis and treatment, enabling healthcare providers to complete complex procedures more efficiently on the first attempt while improving patient outcomes and lab throughput.

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MINNESOTA MEDTEC, INC.

Minnesota MedTec is an FDA-registered, ISO 13485:2003-certified contract manufacturer specializing in precision medical device components and subassemblies. The company provides comprehensive outsourcing services including extrusion, molding, tube processing, and product assembly for interventional cardiology, radiology, neuroradiology, urology, and gastroenterology applications. Core capabilities encompass custom medical tubing, balloons, braided delivery systems, catheters, and molded polymer components manufactured from medical-grade resins. The company serves as a full-service partner from concept through commercialization, offering clean-room assembly, quality assurance, and regulatory compliance expertise. Minnesota MedTec's manufacturing processes include precision extrusion, injection molding, ultrasound tip forming, multi-durometer shafts, and specialized tube processing techniques to support minimally invasive medical device production.

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Medinux (Tianjin) Technologies Co., Ltd.

Medinux (Tianjin) Technologies Co., Ltd is a subsidiary of the Medinux group specializing in medical innovation technology research and new product development with independent intellectual property rights. The company is ISO 13485 certified and operates in a Class 100,000 cleanroom facility. Core product portfolio includes tumor ablation devices, cryopreservation equipment, and tumor ablation detection systems for both domestic and international markets. The organization conducts R&D and manufacturing in strict compliance with GMP standards and has obtained EU ISO 13485 certification. Recent clinical applications include cryoelectrolysis systems for oncology, particularly lung cancer treatment.

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NovaProbe Inc.

NovaProbe Inc. is a US-based manufacturer of surgical products specifically designed for endoscopic procedures, with a primary focus on laparoscopic surgery. All products are FDA-registered and CE-approved. The company specializes in surgical visualization equipment and accessories, including control panels with embedded 4K touch interfaces and HD/4K visualization systems. NovaProbe serves surgeons and gynecologists globally, offering high-quality, affordable devices informed by industry-leading surgical feedback. The company maintains dedicated divisions for medical device manufacturing (R&D), regulatory compliance consulting, and process automation controls for pharmaceutical and chemical industries.

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DESIGN STANDARDS CORP.

Design Standards Corporation is a vertically integrated medical device manufacturer with over 50 years of experience designing and manufacturing disposable and reusable medical devices for leading companies in healthcare. The company specializes in cardiothoracic devices and robotic surgical instruments, leveraging in-house capabilities spanning product design, CAD/Solidworks modeling, injection molding, tooling, and regulatory compliance (ISO 13485:2016). Services include end-to-end product development from concept through production, prototype testing, and manufacturing automation. Core competencies include medical device R&D, product design and development, regulatory assistance, and custom manufacturing of complex surgical instruments and cardiothoracic components.

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Rocamed Inc.

Rocamed Inc. is a Monaco-based medical device manufacturer specializing in innovative, sterile, and disposable products for urology, gynecology, and laparoscopy. Founded in 2009 as part of the PROMEPLA group and now majority-owned by 21 Invest, the company designs and distributes endo-urological devices compliant with European, international, and FDA standards. With 4 manufacturing sites and distribution across 65+ countries, Rocamed serves urologists and gynecologists globally. The company maintains strong clinical engagement through physician collaboration, training programs, and presence at major international congresses including EAU, AUA, and BAUS. Rocamed's product portfolio focuses on minimally invasive urological solutions including laser systems, ureteral stents, stone retrieval instruments, and prostatic devices.

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Tech Medical Services, Inc.

Tech-Medical Services, Inc. is a specialized distributor and manufacturer of surgical devices and operating room equipment based in Nixa, Missouri, with over 30 years of industry experience since 1989. The company focuses exclusively on minimally invasive surgical solutions, offering a comprehensive product line including laparoscopic scope warmers, insufflation and smoke evacuation tubing systems, laparoscopic irrigation pumps, endoscopic retrieval pouches, gamma probe covers, and specialized suction-irrigation products. Operating as a stocking distributor, Tech-Medical emphasizes rapid delivery with same-day turnaround capability, combined with dedicated clinical support and customer service tailored to operating room requirements. The company holds all products to stringent industry standards and serves as a trusted partner for surgical departments and healthcare facilities seeking reliable, quality surgical instrumentation and supplies.

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ICHOR Vascular Inc

ICHOR Vascular Inc. is a medical device manufacturer specializing in minimally invasive clot removal technology for peripheral vascular occlusions. The company develops the iSWEEP platform—an all-in-one endovascular thrombectomy and embolic protection system that modernizes the traditional Fogarty balloon sweep technique. The iSWEEP combines an occlusion balloon, expandable guide catheter with nitinol funnel, and rapid exchange balloon catheter into a self-contained, three-component system requiring no lytics, additional components, or capital equipment. FDA 510(k) cleared products include the iART 7F System for arterial applications and the iDVT 14F System for venous reperfusion. The technology treats vessel sizes from 4mm to 14mm and addresses both arterial and venous clot pathology. Designed for vascular interventionalists, iCHOR's systems aim to simplify peripheral clot removal while reducing procedural complexity, patient trauma, and operative cost compared to surgical thrombectomy or pharmacological thrombolysis.

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eZono AG

eZono AG is a German manufacturer of portable ultrasound systems and needle-guidance technologies founded in 2004. Headquartered in Jena, Thuringia, eZono specializes in empowering non-traditional ultrasound users—particularly anesthesiologists and point-of-care clinicians—by offering affordable, user-friendly sonography solutions with minimal training requirements. The company's flagship products include the eZono® 5000 ultrasound system featuring proprietary eZGuide® needle-navigation technology for real-time needle tracking, the eZSimulator laptop-based training tool, and integrated Cue Cards educational modules. eZGuide® represents a breakthrough in regional anesthesia and interventional ultrasound, enabling free-hand needle navigation without restricting clinicians to conventional in-plane or out-of-plane techniques. The company's mission centers on bringing ultrasound imaging out of niche applications into mainstream clinical workflows while reducing costs, improving patient outcomes, and lowering procedural complications. eZono targets hospitals, anesthesia departments, emergency care, and point-of-care ultrasound programs across Europe and internationally.

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CardioNXT

CardioNXT, Inc. is a medical device company specializing in 3D mapping and navigation systems for treating cardiac arrhythmias, particularly chronic atrial fibrillation. Founded in 2012 and based in Westminster, Colorado, the company develops the iMap System—an electromagnetic tracking and AI-enabled mapping platform that integrates with leading catheter technologies from Boston Scientific, Medtronic, and Abbott, as well as CardioNXT's proprietary MultiLink CS Catheter. The iMap System supports next-generation pulsed field ablation (PFA) navigation with advanced features including contact detection, customized lesion tagging, and field scaling capabilities. CardioNXT enables zero-fluoroscopy 3D mapping procedures, reducing radiation exposure during cardiac electrophysiology interventions. The company has received FDA 510(k) clearance and holds seven patents in cardiac mapping and navigation technology.

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Neptune Medical, Inc

Neptune Medical is a Silicon Valley–based venture-backed medical device manufacturer specializing in proprietary Dynamic Rigidization™ technology for endoscopic applications. The company designs and commercializes thin-walled tubes—including overtubes, catheters, and cannulae—that instantly toggle between flexible and rigid states to enhance procedural control and efficiency. Pathfinder®, the flagship FDA-cleared dynamic rigidizing overtube, is deployed in leading U.S. hospitals and academic medical centers for diagnostic and therapeutic gastrointestinal procedures, including colonoscopies, upper GI bleeds, retrograde enteroscopy, and ERCP. The technology addresses loop formation challenges during endoscopy, improving scope positioning and maneuverability. Neptune Medical is expanding its product portfolio with additional GI-focused solutions.

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MAJiK medical solutions private limited

MAJiK Medical Solutions Pvt. Ltd. is an ISO 13485:2016 certified original equipment manufacturer (OEM) headquartered in Hyderabad, India, specializing in the design, development, and manufacturing of high-quality medical catheter tubing and related components for the global medical device industry. Operating from a 100,000 sq.ft. facility featuring ISO Class 7 and Class 8 clean rooms, dedicated white rooms for extrusion and heat-shrink operations, and ETO sterilization capabilities, MAJiK serves as a comprehensive single-source provider for sterile medical device manufacturing. The company manufactures a diverse portfolio including reinforced tubing (braided, coiled), specialty catheters (aspiration, guided, steerable, angiographic, micro), stent delivery systems, and custom tubing solutions tailored for cardiac electrophysiology, neurovascular interventions, and urology applications. MAJiK provides end-to-end services encompassing device design, component manufacturing, medical device assembly, packaging, and sterilization. With over 100 global customers and presence in multiple countries, the company emphasizes precision engineering, quality assurance, and compliance with international medical device standards.

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Carmafil

Carmafil develops specialized surgical organization solutions for interventional and endovascular procedures. The company manufactures a unique guidewire bowl designed collaboratively by a dually-trained open/endovascular neurosurgeon and an accomplished engineer. This innovative product addresses a critical workflow challenge in catheterization labs and endovascular suites by preventing tangled catheters and guidewires—a persistent problem with conventional wire management systems. Carmafil's solution enables OR staff to maintain organized, efficient instrument management during complex minimally invasive procedures. The product is particularly suited for neurosurgical, vascular, and interventional radiology environments where precise guidewire and catheter handling is essential for procedural success.

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Hobbs Medical Inc

Hobbs Medical Inc. is a leading manufacturer of precision instruments and custom accessories for gastrointestinal and pulmonary endoscopy. Founded in 1982 and headquartered in Stafford Springs, Connecticut, the company specializes in diagnostic and therapeutic endoscopy accessories, including aspiration catheters, forceps, snares, dilators, stents, and scope introducers. ISO 13485 and FDA-registered, Hobbs Medical serves hospitals, medical universities, ambulatory centers, and veterinary facilities with both standard products and rapid custom design/development services. The company offers contract manufacturing and prototyping for major healthcare device manufacturers, emphasizing rapid turnaround, quality compliance, and cost-effective solutions. Privately and proudly Hispanic-owned and woman-managed, Hobbs Medical maintains strong community and employee commitment with low attrition and internal advancement.

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Tangent Endoscopy, LLC

Tangent Endoscopy manufactures the Tangent Digital Catheter System, a single-use flexible endoscope designed for choledochoscopy and biliary duct exploration (CBDE). The system features a 3.28mm outer diameter with a 1.6mm working channel—33% larger than competing systems—enabling enhanced procedural access and stone removal. The catheter delivers 400x400px digital vision with a 120° field of view, supporting both image capture and video via USB. The ambidextrous handle employs an intuitive lever-and-wheel mechanism for 4-axis control. The integrated digital controller offers HDMI outputs, adjustable brightness, and plug-and-play connectivity. FDA 510(k) cleared as of September 2025, the system is positioned for interventional endoscopy and advanced biliary interventions in hospital and specialty centers.

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Creo Medical, Inc

Creo Medical is a UK-based medical device manufacturer specializing in minimally invasive electrosurgical instruments for therapeutic endoscopy. Founded in 2001 and headquartered in Chepstow, Wales, the company designs and markets advanced energy devices utilizing proprietary Kamaptive® Technology, which combines high-frequency microwave and bipolar radiofrequency energy. The product portfolio spans gastroenterology, urology, and pulmonology applications, featuring flagship devices such as the Speedboat Inject (resection), MicroBlate ablation systems, and specialized endoscopic accessories. Creo Medical holds 318 patents globally and operates 14 offices across nine countries. The company has achieved FDA and CE Mark regulatory clearances and demonstrates strong clinical adoption, including NHS supply chain qualification with documented cost savings (£687k over 12 months in pilot programs). The product range encompasses diagnostic tools (biopsy forceps, capsule endoscopy systems), therapeutic instruments (polypectomy snares, extraction devices, hemoclips), and hygiene components for endoscope maintenance.

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DanaMed Inc

DanaMed Inc specializes in orthopedic surgical devices for anterior cruciate ligament (ACL) reconstruction. The company manufactures the Pathfinder™ ACL System, a 3D-printed biocompatible surgical guide that enables anatomically accurate femoral tunnel positioning during ACL reconstruction surgery. The Pathfinder implements the proprietary Hybrid Transtibial Technique, combining advantages of both transtibial and anteromedial portal approaches to achieve >90% overlap with native femoral insertion sites while maintaining knee positioning at 90 degrees of flexion. This minimizes graft tunnel mismatch, reduces hyperflexion complications, and eliminates risk of articular cartilage damage. The device is manufactured using Direct Metal Laser Sintering (DMLS) technology and has been documented in peer-reviewed surgical literature demonstrating optimized biomechanical, kinematic, and clinical outcomes for ACL reconstruction procedures.

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IntroMedic Co., Ltd.

IntroMedic Co., Ltd. is a South Korean medical technology company founded in 2004, specializing in capsule endoscopy systems and minimally invasive endoscopic diagnostic equipment. The company manufactures and markets the MiroCam® Capsule Endoscope System for high-resolution gastrointestinal imaging, the E.G. Scan™ flexible video esophagoscope for esophageal and gastric visualization, and EndoClot hemostasis equipment for bleeding control. IntroMedic holds ISO 13485 certification and FDA 510(k) clearance, serving hospitals and clinics globally with approximately 70 employees. The company is committed to advancing minimally invasive endoscopy solutions for improved diagnostic accuracy and patient outcomes in gastroenterology and related specialties.

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OPCOM Medical Inc.

OPCOM Medical Inc. is an ISO 13485:2016 certified ODM/OEM manufacturer specializing in single-use disposable endoscopes and catheter solutions. Established in 2022 as a subsidiary of OPCOM Group (founded 1993), the company provides comprehensive turn-key solutions from system design, validation, and prototyping through high-volume cleanroom manufacturing. Capabilities span endoscope design, medical camera modules, catheter engineering (including braided, microcatheter, and steerable shafts), thermal bonding, laser welding, and complex sub-assemblies. The company serves cardiac electrophysiology, structural heart, urology, peripheral vascular, and general endoscopy markets. With R&D and manufacturing based in Taiwan and backed by 20+ years of industry experience, OPCOM Medical supports regulatory compliance including 510(k) applications and device validation, enabling customers to accelerate time-to-market for innovative medical devices.

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Opus KSD, Inc.

Opus KSD designs, manufactures, and distributes SubQ It!, an FDA-cleared, ISO 13485-registered bioabsorbable dermal fastener system for surgical wound closure. SubQ It! is a subcuticular stapler that combines the speed of metal staples with the cosmetic results of sutures, without requiring removal or piercing the skin. The device delivers 7X faster closure than traditional sutures and is specifically designed for closing small incisions, laparoscopic trocar sites, and longer surgical wounds (up to 25cm). Available in two product lines—SU-10 and SU-25—it eliminates patient discomfort associated with metal staple removal and reduces operative time. The device is ideal for minimally invasive surgery (MIS) and general surgical applications.

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Nanice Medical Solutions, LLC

Nanice Medical Solutions manufactures the Carpal Clip, a disposable endoscopic carpal tunnel release (ECTR) device designed to improve surgical safety and visualization during carpal tunnel surgery. The device features dual arms that encompass and stabilize the transverse carpal ligament above and below, providing surgeons with a clear operative field while preventing unwanted soft tissue infiltration. The Carpal Clip includes an integrated knife slot for safe, scope-guided ligament transection and is compatible with standard 4mm endoscopes. The single-use device accommodates both unilateral and bilateral procedures and can be used for right or left carpal tunnel release without modification. By securing the ligament in place, the device frees the surgeon's hands to manipulate additional instruments and allows for confirmation of complete ligament release. Designed with safety, efficiency, and accuracy as core features, the Carpal Clip reduces procedural complexity and risk during endoscopic carpal tunnel decompression.

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Dragon Crown Medical Co., Ltd.

Aegis Meditech, Inc. (also known as Aegis Spine) is a physician-centric medical device manufacturer headquartered in Costa Mesa, California, with additional operations in Englewood, Colorado. The company specializes in the development, manufacturing, and distribution of advanced spine implants and fixation devices. Aegis Meditech's product portfolio encompasses expandable lumbar cage systems, cervical plate and fixation assemblies, minimally invasive surgery (MIS) solutions, sacroiliac (SI) joint products, and thoracolumbar devices designed to support fusion and fixation procedures. The company emphasizes innovation in spinal surgery technology, serving orthopedic and neurosurgical practitioners. Products include both functional fusion devices and traditional fusion device platforms across multiple spinal regions.

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Sunny Medical Device (Shenzhen) Co., Ltd.

Sunny Medical is a leading contract manufacturer of medical devices in China, specializing in plastic molding, assembly, packaging, and ETO sterilization services. The company offers SUNMED™ branded products, OEM, ODM, and customized medical device solutions to worldwide customers, with particular expertise in cardiology and radiology intervention products. Sunny Medical manufactures comprehensive PTCA surgery accessories including balloon catheters, inflation devices, guide wires, Y connectors, and related interventional devices. With ISO and CE certifications, the company has established distribution across more than 50 countries, primarily serving markets in the EU, Middle East, and other regions including Germany, Poland, Italy, Turkey, and Iran.

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VITALITEC INT'L., INC. d/b/a Peters Surgical USA

Peters Surgical USA is the American subsidiary of Peters Surgical, a French surgical device manufacturer founded in 1926. The company specializes in designing, manufacturing, and distributing high-performance surgical devices for open and minimally invasive procedures. Core competencies include surgical sutures (developed in collaboration with Professor Alain Carpentier), haemostatic clips and manual ligation systems, temporary occlusion clamps (both reusable metal and single-use), and laparoscopic surgery instrumentation. Products serve cardiovascular, digestive, and uro-gynecological specialties. Peters Surgical USA is the exclusive U.S. distributor of Geister Medizintechnik open and minimally invasive instrumentation. The company emphasizes sterilized, single-use devices with clinical efficacy and safety. With a global presence in over 90 countries and production in the U.S., the organization combines localized manufacturing with international surgical expertise and R&D investment.

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Cardio Flow, Inc.

Cardio Flow, Inc. is a medical device manufacturer specializing in orbital atherectomy systems for the treatment of peripheral artery disease (PAD). The company's flagship product, FreedomFlow, is a modern atherectomy platform featuring diamond-coated rotating spheres designed to efficiently treat complex vascular lesions across a wide range of vessel diameters (2 mm to 8 mm). The platform offers multiple catheter configurations (5 Fr and 6 Fr variants with 3- or 5-sphere driveshafts), adjustable rotational speeds (50K–76K RPM), and single-device versatility for treating multiple blockages and vessel types from ankle to hip. FreedomFlow is designed for use in hospital operating rooms, ambulatory surgery centers, and office-based interventional labs, emphasizing workflow optimization, reduced capital costs, minimal inventory requirements, and rapid physician adoption with a shallow learning curve.

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Nventric, Inc.

Nventric is a contract development and manufacturing organization (CDMO) specializing in end-to-end medical device design, development, and manufacturing for the neurovascular, electrophysiology, and coronary markets. The company serves as a strategic partner to medical device OEMs, providing comprehensive solutions from concept through volume production. Nventric's capabilities span innovative design services, advanced prototyping, rigorous testing, clinical design inputs, and full manufacturing support with ISO 13485 certification. The company develops a broad range of interventional devices including revascularization devices, catheters (balloon, guide, aspiration, diagnostic, and ablation), drug-eluting stents, hemostasis valves, and peripherally inserted central catheters (PICCs). Nventric's focus on complex vascular anatomy navigation and energy delivery systems positions it as a specialized partner for treating vascular diseases across multiple clinical applications.

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Point Robotics MedTech Inc.

Point Robotics MedTech Inc. is a leading developer of surgical navigation systems and robotic-assisted surgery platforms designed to advance minimally invasive orthopedic and neurological procedures. The company specializes in assistive surgical robotics with integrated navigation technologies that enhance surgical precision, safety, and reliability in the operating room. Point Robotics' flagship offering, the Kinguide Agile Robotic Arm Surgical Stereotactic System (Taiwan TFDA-approved), combines real-time trajectory guidance, optical tracking, and broad 3D imaging compatibility to reduce surgical variability and improve patient outcomes. The company emphasizes clinically proven minimally invasive solutions for spinal surgery and related orthopedic applications, with commitment to innovation in robotic-assisted surgical technologies that deliver measurable clinical benefits to physicians and healthcare institutions.

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EndoClot Plus Co., Ltd.

EndoClot Plus Co., Ltd. is a medical device manufacturer specializing in hemostatic solutions for gastrointestinal endoscopy. Based in Santa Clara, California with manufacturing operations in Suzhou Industrial Park, China, the company develops proprietary polysaccharide-based hemostatic systems designed to control bleeding during endoscopic procedures. Their flagship EndoClot® Polysaccharide Hemostatic System (PHS) delivers a biocompatible powder directly to GI tract wounds during endoscopy, enabling rapid hemostasis without thermal or mechanical trauma. The company collaborates with endoscopists and biomaterial scientists to advance therapeutic solutions for GI professionals, offering a pipeline of biomaterial-based devices including adhesive formulations and submucosal injection systems for endoscopic applications.

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Platform Innovations Inc.

Platform Innovations Inc. designs and commercializes specialized surgical accessories for minimally invasive procedures. The company develops innovative solutions addressing clinical pain points in laparoscopic and robotic surgery across multiple surgical specialties. Their flagship product, the ACSIS (Adjustable Curve Suction Irrigation Sleeve), is an advanced accessory engineered to enhance surgical precision, safety, and efficiency in complex procedures. ACSIS features an adjustable curved design, soft blunt distal tip, non-conductive materials, and enhanced visualization capabilities. The device is indicated for colorectal, gynecologic, thoracic, and urologic procedures where improved access, reduced tissue trauma, and optimized field clarity are critical. ACSIS is available in robotic and standard configurations with specified dimensions and catalog numbers for hospital procurement and OR integration.

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Sonivate Medical, Inc.

Sonivate Medical develops innovative fingertip-mounted ultrasound technology that extends clinical ultrasound applications through improved ease of use and accessibility. The SonicEye® Dual Array is a miniature probe combining ultrasound imaging with simultaneous tactile feedback while leaving both hands free for procedural work, addressing the limitations of traditional wheeled ultrasound systems. The company offers a portable system designed for field deployment and forward medical care, particularly for trauma and emergency applications such as eFAST exams. Sonivate's technology targets the $7 billion global ultrasound market, with product applications in anesthesia (peripheral nerve blocks), general surgery, and emergency medicine. The company has received $8.7 million in federal funding through SBIR and BAA programs, including support from the Combat Casualty Care Research Program.

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Agile Devices, Inc.

Agile Devices is a Boston-based medical device development company specializing in innovative steerable and deflectable catheter technologies for interventional procedures. The company's flagship product, the Angler® microcatheter, features active tip control technology that enables clinicians to adjust the catheter tip angle in situ during procedures. This proprietary design reduces the need for device exchanges, thereby minimizing procedure time, radiation exposure, cost, and procedural risk. The technology is particularly valuable in interventional radiology, cardiology, and neuroradiology applications where vessel navigation challenges—such as tortuosity, acute branch angles, and atherosclerotic disease—are common. FDA-cleared for peripheral and coronary vascular use, Agile Devices' steerable microcatheters address critical clinical gaps in catheter navigation, improving outcomes in complex vascular interventions including embolization procedures and coronary angiography.

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MEDCO MFG.

MEDCO MFG is a specialized manufacturer of plastic and cosmetic surgery instrumentation with over 35 years of industry experience. The company is recognized as a leader in liposuction and autologous fat grafting equipment, having collaborated with pioneering surgeons to develop instruments used globally in major hospitals and surgery centers. MEDCO manufactures a comprehensive range of surgical consumables and devices including aspirator systems, cannulas, aspiration and infusion tubing, and post-operative compression garments. Their products are designed for minimally invasive fat transfer and body contouring procedures, serving both hospital and surgical center settings.

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NR Surgical Company

NR Surgical Company is a manufacturer and exporter of high-quality surgical and dental instruments. The company specializes in stainless steel surgical instruments including forceps, scissors, retractors, and trocars for general surgery, orthopedic procedures, and minimally invasive techniques. Product range extends to dental instruments such as scalers and curettes, ENT instruments including rhinology tools, oral maxillofacial surgery instruments, and veterinary surgical instruments. All products are manufactured from premium-grade stainless steel to ensure durability and compliance with medical standards. The company operates as a B2B supplier serving healthcare facilities, dental practices, and surgical centers globally.

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Femasys Inc.

Femasys Inc. is a woman-founded and led biomedical company dedicated to enhancing women's healthcare through innovative, minimally invasive, non-surgical technologies. The company focuses on addressing significant needs in infertility, contraception, and cancer diagnostics. With a mission to provide safe and accessible solutions, Femasys aims to improve patient care and health standards globally, supported by a robust portfolio of approximately 200 patents. The company develops a range of therapeutic and diagnostic products using a proprietary non-surgical delivery platform. Key offerings include FemaSeed, an intratubal insemination device; FemVue, an ultrasound-based diagnostic tool; FemBloc, a candidate for non-surgical birth control; and FemCerv, a tissue sampler for cervical cancer diagnosis. Femasys emphasizes safety and efficiency in its in-office approaches, with a commitment to empowering women throughout their reproductive journeys. The company is publicly traded on NASDAQ under the ticker FEMY.

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RegenMed Systems Inc.

RegenMed Systems Inc. manufactures the MarrowMiner, an FDA-cleared minimally invasive medical device for rapid bone marrow harvesting. The device represents the first significant advancement in bone marrow collection in over 50 years, enabling physicians to harvest bone marrow and marrow-derived stem cells from a single puncture under local anesthesia in 10-20 minutes—4-10 times faster than traditional aspiration methods. The MarrowMiner yields higher quantities of clinically-proven vital stem cell subtypes with greater consistency, supporting applications in bone marrow transplantation, orthopedic procedures, and regenerative medicine. The technology has been clinically validated and published in the Biology of Blood & Marrow Transplantation journal. By reducing procedure time, anesthesia requirements, and operating room utilization, the MarrowMiner simultaneously improves patient outcomes while reducing procedural costs, enabling broader adoption of stem cell-based therapies in both autologous and allogeneic marrow applications.

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Vathin America Co., LTD.

Vathin Medical Instrument Co., Ltd. (also operating as Huaxin Medical) is a leading global manufacturer of disposable electronic endoscopes and minimally invasive surgical instruments. Founded in 2018 and headquartered in Xiangtan, Hunan Province, the company employs over 300 personnel with R&D and sales centers in Berlin and Shanghai. Vathin specializes in innovative disposable endoscope technologies across pulmonology, urology, otolaryngology, and gastroenterology, featuring proprietary riveted snake-bone designs enabling superior articulation (up to 210° bending angles) and precision positioning. The company operates an automated manufacturing facility producing 400,000 units annually with ISO certifications and over 200 patent applications. Vathin products are FDA and CE approved, distributed across 160+ countries, and marketed through strategic partnerships including Olympus. Product portfolio encompasses disposable bronchoscopes, cystoscopes, ureteroscopes, rhinolaryngoscopes, and complementary minimally invasive surgical instruments including laparoscopic staplers and ultrasonic energy devices. The company addresses clinical demand for infection-free, cost-effective alternatives to reusable instruments while supporting graded diagnosis and treatment protocols.

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Route 92 Medical

Route 92 Medical is a neurovascular intervention medical device company headquartered in San Mateo, California, specializing in endovascular thrombectomy solutions for acute ischemic stroke treatment. The company develops proprietary catheter systems and delivery technologies designed to overcome critical limitations in current neurointervention approaches, including poor navigability through tortuous anatomy, prolonged procedure times, and high failure rates in reaching target lesions. Route 92 Medical's product portfolio includes the FreeClimb Catheter Systems (FreeClimb 54, 70, and 88) powered by Tenzing delivery technology, and the HiPoint Reperfusion System featuring the Monopoint Approach for streamlined super-bore aspiration delivery. These integrated solutions serve interventionalist clinicians and hospitals performing neurovascular procedures, offering comprehensive platforms that eliminate the need for device workarounds and enhance procedural efficiency and clinical outcomes in stroke intervention.

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Total Vein Systems

Total Vein Systems is a comprehensive vein surgery supply distributor founded in 2003. The company markets over 372 products specifically designed for venous intervention and phlebology procedures, including endovenous laser systems, laser fibers with standard SMA connectors, vascular access introducers, infiltration tubing and syringe delivery kits, microphlebectomy surgical instruments, compression hosiery, and associated procedural packs. All products are manufactured to ISO 13485 and KEMA standards. Total Vein Systems serves as a complete supply source for vascular surgeons, interventional radiologists, and phlebologists, positioning itself on quality components, extensive product selection, and competitive pricing.

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C

C-Clear LLC

C-Clear LLC manufactures intra-abdominal lens cleaning products designed for minimally invasive surgery. The company's primary offerings are the C-Clear™ Sleeve and C-Clear™ Baton—standalone lens cleaners that enable surgeons to clean laparoscopic and robotic camera lenses without removing the scope from the body cavity. This approach maintains operative field orientation and reduces OR time by 5–10 minutes per case while cutting lens-cleaning costs by approximately two-thirds. The devices achieve lens cleaning in under 15 seconds, helping surgical teams maintain clear imaging throughout procedures while improving operational efficiency and reducing overall case expenses. C-Clear products are developed by surgeons with over 50 years of laparoscopic operating experience, emphasizing simplicity and clinical practicality.

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Torax Medical Inc.

Torax Medical is a privately held medical device manufacturer specializing in minimally invasive surgical implants for gastrointestinal and pelvic floor disorders. The company's proprietary Magnetic Sphincter Augmentation (MSA) technology uses interlinked titanium beads with magnetic cores to restore sphincter function and barrier integrity. The flagship LINX® Reflux Management System is a laparoscopic magnetic implant that enhances lower esophageal sphincter function to treat gastroesophageal reflux disease (GERD) in patients seeking alternatives to continuous proton pump inhibitor therapy. Long-term clinical data demonstrates 99% of LINX patients report no regurgitation at 5 years, with 85% discontinuing daily PPI use. The company also offers the FENIX® Continence Restoration System, the only FDA-approved surgical implant for fecal incontinence. Both devices emphasize physiologic function preservation, allowing patients to belch and vomit naturally. Torax Medical provides comprehensive physician education, surgical training materials, and patient communication resources to support clinical adoption and patient outcomes in gastrointestinal surgical care.

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Galvanize Therapeutics

Galvanize Therapeutics is a medical device company specializing in Pulsed Electric Field (PEF) energy-based systems for therapeutic interventions. Following the 2023 merger of Gala Therapeutics, Galvanize Therapeutics, and Galaxy Medical, the company now operates the Aliya® PEF System platform. The company develops disease-modifying bronchoscopic and interventional therapies targeting chronic bronchitis, non-small cell lung cancer, metastatic solid tumors, and cardiac arrhythmias. The Aliya® system utilizes non-thermal pulsed electric fields to ablate tissue and modulate biologic processes, with recent clinical data demonstrating local tumor control and potential immune response induction in lung cancer patients. The company also previously developed the RheOx™ Bronchial Rheoplasty System for reducing mucus-producing cells in chronic bronchitis. Galvanize serves interventional pulmonologists, thoracic surgeons, and oncologists, with focus on minimally invasive, energy-based therapeutic delivery.

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WEIHAI KAIBO MEDICAL DEVICE CO., LTD.

Weihai Kaibo Medical Device Co., Ltd. is a Chinese medical device manufacturer founded in 2019, specializing in minimally invasive surgical instruments and endoscopic systems. Located in Weihai Medical Devices and Biopharmaceutical Industrial Park, the company is a national high-tech enterprise and member of the National Surgical Instruments Standardization Technical Committee. The company develops and manufactures innovative microinvasive surgical medical devices designed to work with endoscopic technology. Product portfolios span three major clinical areas: laparoscopic surgery, urological surgery, and gastrointestinal endoscopic diagnosis and treatment. The company holds 19 utility patent authorizations and participates in formulating national medical device standards. Recent product certifications include EU compliance certifications for disposable negative pressure drainage bags and suction connection tubing from German TÜV Rheinland.

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PENLON LTD.

Penlon Ltd is an ISO 13485:2016-certified British medical device manufacturer founded in 1943 in Oxford, England, with headquarters in Abingdon, Oxfordshire. The company specializes in the design, manufacture, and global distribution of anaesthesia systems, airway management devices, and endoscopic accessories. Penlon's portfolio includes advanced anaesthetic machines, video laryngoscopes, vaporizers, oxygen delivery systems, suction equipment, and single-use endoscopy instruments (polypectomy snares, hemostasis clips, biopsy forceps). The company also produces MRI-compatible medical devices and offers comprehensive clinical support services. With over 80 years of innovation and four Queen's Awards for Enterprise, Penlon exports to more than 90 countries worldwide and maintains strong connections with the University of Oxford's Nuffield Division of Anaesthetics. The company is recognized for intuitive user interface design, product durability, and reliability in critical care and surgical environments.

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Plasma Surgical Inc

Plasma Surgical Inc manufactures PlasmaJet, an advanced surgical platform that delivers pure-plasma energy for soft tissue dissection, cutting, coagulation, and vaporization in open and videoscopic (minimally invasive) procedures. The PlasmaJet System comprises a console unit that generates and delivers gas and energy, and interchangeable handpieces that emit a controlled, rapidly dissipating stream of pure plasma. The technology is designed to enable precise tissue removal while minimizing lateral thermal spread and deep penetration, thereby preserving surrounding healthy tissue. Primary clinical applications include gynecological surgery (endometriosis, ovarian conditions) and oncologic procedures (ovarian cancer, bowel and diaphragm resection). The company maintains a global distribution network across the USA, Europe (19 countries), and Australasia. US headquarters are in Roswell, Georgia, with additional regional offices in the UK and France. Products are indicated for use in both open surgical and videoscopic procedures. The company emphasizes surgeon feedback and long-term clinical outcomes data to support product efficacy and safety.

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XPress BCD LLC

XPress BCD LLC manufactures the XPress BCD™ (Breast Compression Device), a reusable medical device designed for use with stereotactic biopsy platforms. The device applies temporary focal mechanical compression to stereotactic breast biopsy sites to achieve hemostasis and reduce post-biopsy hematoma formation. The XPress BCD is a thermoplastic, modular unit available in three geometric configurations, each compatible with standard biopsy paddle systems. Clinical data demonstrates a 70% reduction in hematoma incidence (7.5% vs. 25.4-43% with manual compression) and 50% reduction in hematoma size. The device is reusable, requires only low-cost disposable latex-free covers, and provides operational efficiencies including approximately 11 minutes of labor savings per biopsy procedure. It eliminates ergonomic strain on clinical staff during post-biopsy compression and maintains accurate collinearity of bleeding sites. Patient satisfaction ratings exceed 97% (good-to-excellent). The device is FDA-cleared and intended for breast biopsy applications in interventional radiology and surgical settings.

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TTI Medical

TTI Medical, established in 1984, designs and manufactures high-quality surgical instruments and medical devices, with specialization in video and digital camera adaptation systems. The company serves ophthalmology, surgical microscopy, and endoscopy markets by providing optical coupling solutions that integrate modern imaging technology with existing clinical equipment. Primary product lines include C-mount video adapters for surgical microscopes and slit lamps, digital camera adapters, endoscope couplers with 4K optical performance, CO₂ laser accessories (micromanipulators, handpieces, laparoscope couplers), fiberoptic handpieces for contact laser procedures, reusable suction/irrigation instruments for minimally invasive surgery, and medical-grade video camera systems (including the Ikegami MKC-X800 Native 4K). TTI Medical is an authorized distributor of Ikegami, Sony, and Jena Surgical products. All products are manufactured in the USA and are reusable and sterilizable. The company holds FDA registration, CE mark approval, and ISO 13485:2016 certification. TTI Medical also provides OEM solutions including custom engineering, private labeling, and laser engraving services.

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