In the rapidly evolving landscape of orthopedic surgery, Endobuttons have transitioned from niche components to fundamental elements of ACL and PCL reconstruction. As a professional OEM manufacturer, we recognize that the critical success factor in ligament fixation is not merely the device, but the interplay between biomechanical integrity, material science, and surgical ease-of-use.
Global procurement trends indicate a shift towards minimally invasive surgical techniques. Hospitals and distributors are demanding implants that reduce operation time while maximizing bone-tendon healing interface. Our custom OEM capabilities ensure that surgeons receive devices that match specific patient anatomies, backed by rigorous fatigue testing and material validation.
Post-pandemic, the orthopedic supply chain has emphasized localization and traceability. We bridge the gap between high-tech manufacturing and clinical delivery. By integrating ISO 13485 standards and strict FDA/CE compliance pathways, we provide global partners with a "turn-key" manufacturing solution that mitigates cross-border regulatory risks.
Our R&D department is currently focusing on bio-resorbable polymers and enhanced titanium surface treatments that promote faster osteointegration. By investing in 3D prototyping and AI-driven stress analysis, we ensure our clients stay ahead of the competitive curve in the orthopedic instrument market.
Founded in 2001, Chengdu Medev Medical Instruments Co., Ltd. represents two decades of specialized orthopedic innovation. Spanning over 18,000㎡, our facility is not just a factory—it is a hub of precision medical engineering.
Cleaned implants ensure a reduction in post-operative infection risks, guaranteeing patient safety during complex surgeries.
Simulating human body tensile forces through rigorous material yield strength and elongation testing protocols.
Advanced heat-sealing and sterile barrier systems to ensure implant integrity from our workshop to the operating theater.
Our OEM Endobuttons are manufactured using medical-grade Titanium and PEEK, utilizing advanced CNC machining for precise geometry. They are engineered to provide maximum fixation strength for ligament grafts while minimizing surgical trauma.
We operate under strict ISO 13485 standards. We provide a full Technical File, including material certifications, sterilization validation, and biomechanical test reports, supporting your local registration processes.
With an 18,000㎡ manufacturing capacity, we maintain agile production lines. From prototype validation to mass production, we work closely with our partners to provide transparent timelines, typically ranging from 4 to 8 weeks depending on customization complexity.







