Bonevia
Bonevia
Explore our foundational range of surgical implants, clinical fixation sets, and osteosynthesis systems engineered to global specifications.
The shift toward minimally invasive surgery (MIS) has transformed orthopedic trauma treatments. Standard solid screw mechanisms often limit precision positioning, leading to sub-optimal reduction and prolonged operating times. Titanium Cannulated Screws mitigate these complications by allowing guide-wire directed placement, ensuring absolute alignment before definitive implantation.
As a professional manufacturer, Bonevia leverages high-grade biocompatible titanium alloys (Grade 5 / Ti-6Al-4V ELI) complying with ISO 5832-3 and ASTM F136 specifications. Our advanced cannulated profiles optimize strength-to-weight performance while preserving inner canal hollow integrity, avoiding structural compromise during torque stresses.
Subjected to exhaustive torsional, axial-pullout, and fatigue tests in accordance with ASTM F543 requirements. Our cannulated screws reduce the risk of intra-operative breakage to near-zero.
Our Type II / Type III anodizing process produces an bio-inert titanium oxide layer, maximizing corrosion resistance and preventing metal-ion leaching inside the physiological environment.
Evaluating macro-demand dynamics, global distributor requirements, and international regulatory frameworks for Class III orthopedic implants.
We work closely with 850+ medical distribution networks across Europe, Southeast Asia, the Middle East, and South America to maintain a steady inventory of surgical-grade implants.
Our processing environment operates under ISO 13485 quality systems. We manage meticulous traceability files, material mill certificates, and biocompatibility protocols to support local CE / FDA clearance registration.
We transform proprietary customer concepts into clinically viable products. Supported by our 85-engineer R&D center, we offer customization of pitch, diameter (2.0mm to 7.3mm), length, and drive configurations.
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㎡ (specialized cleanroom and high-precision CNC machining center), Bonevia maintains strict quality management standards and efficient manufacturing processes. The company records an annual export revenue of around USD 8–15 million, supported by 6 years of export experience and over 10 years of overall industry experience.
Quality assurance is a core focus at Bonevia. The company implements multiple inspection methods including incoming material inspection, in-process quality control, and final product testing, supported by a dedicated quality team of 35 professionals. This ensures all products meet international medical device standards.
In the past year, Bonevia successfully launched 120 new product designs, supported by a research and development team of 85 engineers, continuously driving innovation in orthopedic implant systems and surgical instruments. Our trade ecosystem relies on diversified global distribution networks, serving hospitals, clinics, and medical distributors across Europe, Southeast Asia, the Middle East, and South America with over 850 partners.
A step-by-step overview of our specialized engineering workflows, utilizing advanced machinery to execute medical-grade orthopedic implants.
Ensuring cross-border medical compliance, localized technical assistance, and stable documentation pipelines for distributors.
Regulatory pathways for Class III implants require detailed Technical Files. Bonevia provides direct access to biological evaluation records, biocompatibility test results (ISO 10993), chemical characterization studies, and validation documents for sterilization cycles.
We maintain full traceability back to raw titanium ingots. This documentation helps minimize delays with regional regulatory bodies (such as EMA, COFEPRIS, ANVISA, and TFDA).
"Our logistics operations handle complete custom clearances, offering door-to-port medical product delivery, reducing regional supply bottlenecks."
Our production environment is regularly monitored for bioburden and airborne particulate levels, ensuring high hygiene standards before sterilization packaging.
Our regulatory support team assists with tender documentation, local product certifications, and custom translation of surgical manual guides.
Providing high-precision stabilization across varying anatomical regions for human and veterinary orthopedics.
Using parallel groupings of large-diameter cannulated screws (6.5mm / 7.3mm) to provide mechanical stability, compression, and anti-rotational control for elderly and active trauma patients.
Micro-sized options (2.0mm / 2.7mm / 3.0mm) are used for distal radius, hand, and scaphoid osteosynthesis, securing small bone fragments with minimal soft tissue disruption.
Specialized veterinary configurations address canine tibial plateau leveling osteotomies (TPLO) and feline fracture fixations, designed to withstand unpredictable postoperative loading forces.
At Bonevia, we monitor ongoing innovations in biomaterial science and implant manufacturing. Our R&D team works on advanced surfaces, including magnesium-based biodegradable materials and osteoinductive coatings.
Additionally, we are investigating 3D-printed titanium implants with porous structures designed to mimic natural trabecular bone, which may support improved long-term integration.
By combining CAD simulation with clinical feedback from our global distribution network, we continue to develop systems that support patient recovery and help simplify surgical procedures.
Expert answers addressing materials, quality control, customization tolerances, and regulatory documentation requirements.
We use Ti-6Al-4V ELI (Extra Low Interstitial) alloy conforming to ASTM F136 and ISO 5832-3. This grade offers high biocompatibility, high fatigue strength, and a lower modulus of elasticity compared to stainless steel.
Concentricity is monitored using deep-hole gun-drilling systems on Swiss-type lathe machinery. Our quality inspection team, consisting of 35 professionals, checks concentricity during production using high-resolution video measuring systems and optical comparators to maintain a tolerance of ±0.02mm.
Supported by our 85-member R&D team, we customize diameters (from 2.0mm to 7.3mm), drive patterns (hexagonal, torx, star), thread configurations (fully-threaded, partially-threaded), and pitch types. We also offer custom anodization colors for easy identification during surgical procedures.
We supply raw material test reports (Mill Certificates), packaging integrity validations, sterilization validations, biocompatibility evaluation documents, and ISO 13485 quality system certificates to help streamline local registration procedures.
Explore our corresponding spine stabilization, orthopedic power tools, and trauma fixation assemblies designed to complete your surgical supply pipeline.
