Bonevia
Bonevia
Engineered for high-load bio-compatibility, stability, and precise clinical insertion
Poland's healthcare infrastructure has undergone massive modernization over the last decade. Driven by the National Health Fund (NFZ - Narodowy Fundusz Zdrowia) updates, public and private clinical institutions across Warsaw, Kraków, Poznań, and Gdańsk are demanding higher medical device compliance. Transitioning from legacy rigid fixation products to advanced minimally invasive osteosynthesis has dramatically accelerated the demand for high-strength, biocompatible cannulated screws.
Polish medical procurement teams face a dual pressure: optimizing tender budgets while strictly complying with the European Union Medical Device Regulation (EU MDR 2017/745). High-quality titanium alloy cannulated screws (specifically 6.5mm, 4.5mm, and headless micro-compression variants) are widely utilized in Polish hospitals for femoral neck fractures, scaphoid stabilization, and calcaneal reconstructions. Working directly with an established global manufacturer like Bonevia allows Polish distributors and hospital groups to secure a reliable, high-volume supply chain that bridges the gap between premium mechanical performance and reasonable cost structures.
Cannulated screws represent a major mechanical shift in fracture fixation. By utilizing a hollow core, surgeons can insert a precise K-wire (Kirschner wire) under fluoroscopic guidance to map the path before drilling and driving the screw. This drastically reduces the probability of bone misalignment or cortical blowout.
At Bonevia, our cannulated screws are manufactured utilizing premium medical-grade Titanium Alloy (Grade 5, Ti-6Al-4V ELI) conforming to ASTM F136 and ISO 5832-3 standards. This material delivers a modulus of elasticity closer to cortical bone compared to traditional stainless steel, significantly decreasing stress-shielding risks. The self-tapping and self-drilling thread profiles feature optimal pitch density designed to maximize pull-out strength in both osteoporotic and high-density cancellous bone tissues.
Engineered to deliver exceptional mechanical performance in demanding clinical scenarios.
Bonevia Orthopedic Technology Co., Ltd. — Delivering Clinical Excellence Since 2015
Bonevia Orthopedic Technology Co., Ltd. is a professional manufacturer specializing in orthopedic implants and surgical solutions, dedicated to advancing innovation in trauma, spine, and joint reconstruction products. Since its establishment in 2015, the company has grown steadily into a trusted supplier in the global orthopedic industry.
With a modern production facility covering approximately 320㎡, Bonevia maintains strict quality management standards and efficient manufacturing processes. Supported by 6 years of export experience and over 10 years of overall industry experience, we ensure that every batch of trauma implants complies with local European import standards.
Quality assurance is our core focus. We implement multiple inspection methods including incoming material inspection, in-process quality control, and final product testing, supported by our dedicated team of 35 QC professionals. Our global distribution network proudly serves major markets across Europe, Southeast Asia, the Middle East, and South America with a robust supply chain ecosystem consisting of more than 850 partners.
Navigating the regulatory matrix is the single largest hurdle for medical distributors in the European Union. At Bonevia, we have aligned our design, raw material sourcing, and cleanroom packaging operations with the strict frameworks of ISO 13485:2016 and the European Medical Device Regulation (MDR). This means every implant shipped to Poland contains the necessary technical documentation, traceability data, and sterile processing verification.
Furthermore, we support Polish distributors with the required documentation for local notifications to the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products (URPL - Urząd Rejestracji Produktów Leczniczych, Wyrobów Medycznych i Produktów Biobójczych) in Warsaw. We provide complete technical files, biocompatibility certificates (ISO 10993), sterilization validation details, and instruction manuals translated to facilitate seamless approval processes.
Extensive orthopedic solutions designed for spinal, extremity, and articular interventions
Reliable performance for complex bone osteotomies and specialized animal clinical care
The future of osteosynthesis implants lies in reducing secondary removal surgeries and improving osseointegration. Bonevia's current R&D pipeline is exploring magnesium-based bioabsorbable cannulated screws and customized 3D printed porous titanium implants. Over the next three to five years, clinical applications will transition toward custom-fit implants mapped through preoperative CT scans.
By establishing relationships with Polish researchers and clinical experts today, we aim to integrate local research feedback into our design optimization. Our engineering team of 85 staff members works dynamically to ensure that we maintain high technological standards, constantly updating our instrumentation kits and screw thread profiles to match the latest anatomical data.
Essential guidance for Polish medical distributors, hospital purchasing managers, and surgeons