Surgical Instruments in North Carolina

WestBridge Vocational is an FDA-registered social enterprise manufacturing facility specializing in disposable medical devices. The company produces surgical drapes and wraps for leading medical suppliers and distributors. Additionally, WestBridge offers custom medical sewing services, including catheter covers, shoulder stabilizers, medical equipment coverings, and neonatal medical products. The facility operates as a controlled-environment manufacturing center serving domestic and international markets. Beyond manufacturing, WestBridge provides vocational rehabilitation program services and employment training for adults and youth with barriers to employment, operating under contract with the North Carolina Division of Vocational Rehabilitation. The company supports over 100 participants in job skills development and employment marketability enhancement. As a mission-driven manufacturer, WestBridge combines quality-driven production with workforce development, positioning itself as a contract manufacturing partner for B2B medical supply companies seeking domestic USA manufacturing capacity with trained workforce support.

Asensus Surgical, Inc. is a medical device company specializing in robotic-assisted surgical systems and augmented intelligence solutions for the operating room. The company manufactures the Senhance® Surgical System, a robotic platform designed to provide surgeons with enhanced control, precision, and real-time decision support during minimally invasive procedures. The Senhance system features an innovative open ergonomic design that improves surgeon communication and physical comfort while maintaining intra-operative control. A cornerstone of Asensus's technology is the Intelligent Surgical Unit™ (ISU™), an intra-operative augmented intelligence system approved globally that delivers real-time surgical insights to enhance decision-making, reduce variability, and improve procedural outcomes. The ISU represents the company's Performance-Guided Surgery™ platform, which layers advanced robotics with reusable 3mm and 5mm articulating surgical instruments to extend safer, more predictable surgical care beyond traditional robotic-assisted surgery models. Asensus markets its systems to hospital operating rooms, surgical centers, and healthcare institutions globally, targeting surgeons seeking to perform safer, more accessible robotic-assisted procedures. The company has received multiple industry recognitions including Digital Health Awards and Surgical Robotics Industry Award nominations. While specific FDA 510(k) status and detailed regulatory certifications are not explicitly stated in available content, the site indicates the ISU is approved for use globally, suggesting appropriate regulatory clearances. The company is headquartered in Durham, North Carolina, and maintains an international team of physician partners and clinical collaborators.

KMD Surgical Solutions, Inc. manufactures K-LOCK™, a patented sutureless surgical drain securement device designed to improve patient comfort and reduce drain-related adverse events. The device uses a braided sleeve mechanism that functions like a Chinese finger trap, securing drains without the pain and skin irritation associated with traditional suture-based methods. The K-LOCK™ features a rotary retainer that holds drain tubing parallel to the skin and allows repositioning to avoid pressure points and clothing interference (Control Your Comfort™ positioning). The company reports that approximately 50 million surgical drains are placed annually in the U.S., with current suture-based securement methods resulting in high rates of patient complaints regarding pain, skin irritation, and impact on activities of daily living. A clinical study published in Plastic Surgery Global Open (2025) conducted at Wake Forest School of Medicine's Department of Plastic Surgery demonstrated that K-LOCK™ reliably secured drains, could be applied faster than sutures, caused no adverse events, and resulted in statistically significant patient preference across all measured categories: maintenance/care, activities of daily living, skin irritation, itching, tugging, overall pain, and overall experience. The device addresses a significant clinical need in post-operative care by reducing inadvertent drain loss (which can cost $5,000–$35,000 per event and require hospital readmission or return to OR) and improving patient quality of life during recovery.

H.B. Fuller Medical Adhesive Technologies is a medical adhesive manufacturer serving both medical professionals and medical device manufacturers. The company develops and supplies a comprehensive range of high-performance adhesive solutions for surgical, wound closure, vascular access, and infection prevention applications. Their product portfolio includes cyanoacrylate-based surgical adhesives (Glubran® 2 line in multiple sizes), topical skin adhesives (SurgiSeal® and SurgiSeal Stylus®), catheter securement adhesives (SecurePortIV®), and microbial sealants (FloraSeal®). H.B. Fuller serves medical professionals requiring safe and effective surgical and wound closure adhesives, as well as medical manufacturers seeking adhesive components for device assembly, skin-contact applications, personal protective equipment (PPE), and medical filtration. The company emphasizes regulatory compliance, safety, efficacy, and comfort in all formulations. Products are designed to enhance patient care outcomes and streamline medical procedures. The organization positions itself as a trusted partner committed to advancing healthcare through adhesive innovation and science-based solutions.

Teleflex Incorporated is a NYSE-listed (TFX) global medical technology company headquartered in Morrisville, North Carolina. The company designs, manufactures, and distributes innovative medical devices and solutions across multiple clinical specialties including anesthesia, emergency medicine, interventional cardiology and radiology, interventional urology, surgical care, general urology, and vascular access. Teleflex serves healthcare professionals and patients through a diversified portfolio of critical care and procedural products. The company recently completed the acquisition of BIOTRONIK's Vascular Intervention Business, expanding its interventional capabilities. Key product areas include anesthesia delivery systems, emergency airway and resuscitation equipment, catheterization laboratory instrumentation, urological devices (including the UroLift system), surgical instruments and staplers (such as the Titan SGS stapler for bariatric surgery), and vascular access devices. Teleflex also serves military and federal healthcare markets. The company operates Teleflex Academy, a comprehensive education platform providing training and professional development for healthcare organizations and clinicians. Teleflex maintains significant research and development capabilities with multiple design centers, supporting ongoing innovation in medical device technology. The company is recognized as a Forbes Best Employer for Engineers (2025) and received the VETS Indexes Recognized Employer Award for the second consecutive year, reflecting its commitment to recruiting and supporting veterans. Manufacturing and service capabilities span multiple geographic locations, with strong regulatory and quality management systems supporting FDA, ISO, and international compliance requirements.

Exotoe LLC manufactures ExoToe™, a next-generation extramedullary hammertoe fixation device designed to address limitations of traditional K-wire fusion and intramedullary fixation approaches. The ExoToe™ implant is a precision surgical device measuring just 0.6mm in thickness that preserves the medullary bone canal, eliminating the need for intramedullary canal insertion. It features interoperative anatomic angle adjustability, allowing surgeons to achieve straight or customized angle correction during the procedure. The device is available in three sizes (5.5, 6.5, and 7.5mm) and is crafted from premium 316 stainless steel. Key competitive advantages include rotational stability at the proximal interphalangeal joint fusion site, compatibility with supplemental K-wire fixation across the metatarsophalangeal joint, ease of implantation using standard crimping forceps, and reversibility through Mini-Hohmann retractor removal if needed. ExoToe™ is indicated for primary hammertoe correction and revision cases. The company is also developing ExoClip™, a complementary implant solution. Exotoe LLC partners with Surgical Design Innovations, which brings extensive medical device development expertise including product design, mechanical and cadaveric testing, and early clinical evaluation. The device is supported by a detailed surgical technique guide and has received positive feedback from podiatric surgeons regarding ease of use and fusion site stability.

Uro1 Medical manufactures precision biopsy instruments and specimen handling solutions for targeted tissue sampling. The company's SUREcore® core needle biopsy system delivers larger, higher-quality tissue cores with superior architectural preservation, reducing diagnostic ambiguity and the need for repeat procedures. The complementary coreCARE® specimen retrieval technology minimizes tissue handling, fragmentation, and artifact during transfer to histopathology, improving diagnostic accuracy and enabling reliable genomic profiling. Solutions are designed for urology and oncology practices seeking to enhance biopsy adequacy and reduce procedural delays.

Tobra Medical is a specialty medical device company founded in 2015, headquartered in Wake Forest, North Carolina. The company designs and manufactures innovative single-use disposable devices for autograft bone and specimen collection during surgical procedures. Their product portfolio includes the Tobra Bone Basket for simplified collection of autologous bone particles during drilling, the Tobra Specimen Basket for sterile specimen handling, and FeatherFlow tubing for enhanced bone and specimen management. Tobra Medical focuses on user-friendly, economical solutions developed in collaboration with surgeons, medical engineers, and OR personnel to improve clinical efficiency and patient outcomes across orthopedic, neurosurgical, ENT, and oral-maxillofacial surgical specialties.

Custom Medical Specialties manufactures FDA-registered (1063382), ISO 13485-certified disposable medical devices in a Class 8 cleanroom facility in Pine Level, North Carolina. The company specializes in sterile and non-sterile tubing sets (infiltration, aspiration, injection lines), universal drain bags, and custom pre-assembled procedure kits for IV therapy, urology, plastic surgery, and imaging applications. Products are assembled, packaged, and sterilized in-house with full 21 CFR Part 820 compliance. Beyond standard offerings, the company provides contract manufacturing, private labeling, and custom configurations tailored to healthcare provider specifications. With 30 years of operational experience and relationships with 43,000+ healthcare facilities, Custom Medical Specialties emphasizes supply chain reliability, same-day shipping capability, and direct customer support.

Foothills Industries is a CARF-accredited manufacturer specializing in custom surgical drapes and medical packaging. The company operates as a social enterprise, combining medical manufacturing with comprehensive vocational rehabilitation and employment services for adults with disabilities and other barriers to employment. FDA-registered for medical device production, Foothills offers custom surgical drape production, medical packaging and assembly, rework services, and capacity/niche product solutions. The organization provides job training, life-skills training, and community services while delivering quality medical products at competitive costs with reliable on-time delivery.

Gilero is a contract development and manufacturing organization (CDMO) specializing in the design, development, and manufacturing of medical devices and drug delivery systems. Founded in 2002 and headquartered in Durham, North Carolina, Gilero became part of the Sanner Group in September 2024, expanding its global capabilities. The company offers comprehensive end-to-end services across the entire product lifecycle, including design and engineering, concept development, prototyping, clinical and small-batch manufacturing, electromechanical systems integration, human factors and usability engineering, regulatory affairs support, and full-scale contract manufacturing. Gilero operates over 300,000 square feet of ISO-certified cleanroom manufacturing facilities (ISO Class 7 and 8) across North America, Europe, and Asia, enabling both small-batch and high-volume production. With more than 130 engineers and regulatory experts, Gilero supports device development from initial concept through commercialization, serving diverse therapeutic areas including closed-system drug transfer devices, surgical instruments, ocular implant delivery systems, and hemostasis devices. The company combines expertise in biomedical, mechanical, electrical, and software engineering to deliver scalable manufacturing solutions tailored to client specifications and regulatory requirements.