In the evolving landscape of orthopedic trauma surgery, the Headless Cannulated Screw represents a pinnacle of biomechanical design. Unlike traditional cortical screws, the headless design allows for total intra-articular insertion, minimizing soft tissue irritation and eliminating the need for future hardware removal in many clinical cases. As a leading Custom OEM Headless Cannulated Screws Supplier, we understand that precision is not just a requirement—it is a surgical necessity.
Our screws utilize a sophisticated differential thread pitch between the leading and trailing edges. This creates a natural compression force as the screw is advanced, drawing bone fragments together with calculated Newtons of force.
Designed for minimally invasive surgery (MIS), the hollow central core allows for precise placement over a guide wire. This ensures anatomical alignment even in complex intra-articular fractures of the scaphoid, talus, or femoral neck.
Utilizing Medical Grade Titanium Alloy (Ti6Al4V ELI) and Cobalt-Chrome, our implants offer superior fatigue resistance and biocompatibility, meeting strict ASTM and ISO standards for permanent implants.
Years of Export Expertise
Senior R&D Engineers
Market Share in South America
13485 Certified
KaiSo has established a complete Quality Assurance System to continuously fulfil the requirements according to ISO9001, 13485, CE, ranging from material procurement to design development and automated production processes. Our 29,523㎡ facility is a testament to China's advanced manufacturing capabilities in the medical sector.
Our certifications including MDD 93/42/EEC and the latest MDR (Medical Device Regulation) standards ensure our partners can confidently import into European and North American markets.
Choosing a China-based OEM Exporter for Headless Cannulated Screws offers more than just cost efficiency. It is about a vertically integrated ecosystem that accelerates time-to-market for global medical brands.
We provide full regulatory dossier support (technical files) for local registrations. Whether it’s ANVISA in Brazil, FDA in the USA, or CE in Europe, our documentation team ensures seamless compliance.
With 59 R&D engineers, we can move from a CAD drawing to a biocompatible titanium prototype in record time, supporting rapid clinical trials and surgeon feedback loops.
Our automated CNC production lines allow for "High-Mix, Low-Volume" orders, enabling smaller medical distributors to compete with industry giants without holding massive inventory.
The industry is moving toward Smart Implants and Patient-Specific Instrumentation (PSI). As a forward-thinking exporter, we are investing in:
Developing bioactive surfaces that promote faster osseointegration, reducing the patient's recovery time from months to weeks.
Exploring additive manufacturing for custom headless screws that match bone density, reducing the risk of stress shielding.
Transitioning to biodegradable and recyclable sterile packaging systems to meet global ESG requirements for hospitals.