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  • We are a specialized enterprise engaged in the R&D, design, production, sales, and technical services of orthopedic medical devices.
  • Our main products include limb orthopedic external fixators, foot and ankle surgery and pediatric orthopedic internal fixation devices, adult trauma solutions, spinal implants, intramedullary nails, and surgical instruments.
  • We hold ISO 13485 certification and have passed the assessment for China's Good Manufacturing Practice for Implantable and Sterile Medical Devices.
  • Hospitals, orthopedic clinics, distributors, and research institutions.
  • No, we only sell to companies or institutions with legal entity status.
  • We offer both standardized instruments and customized surgical instruments tailored to specific needs.
  • They incorporate biomimetic design, minimally invasive approaches, and surface treatments that promote osseointegration, aligning with international mainstream products.
  • Standard-compliant titanium alloys, stainless steel, aluminum alloys, carbon fiber, and PEEK materials.
  • No adverse feedback has been reported during long-term clinical use.
  • Verified irradiation sterilization shielding system.
  • We can align with hospital procurement procedures. Typically required documents include product registration certificates, manufacturing/distribution licenses, technical specifications, clinical data, and compliance documentation—subject to local regulations.
  • You must possess valid medical device business qualifications and a mature sales and service team. Cooperation can commence after passing qualification reviews, completing business negotiations, and signing an authorization agreement.
  • We offer professional clinical technical support covering preoperative communication, intraoperative assistance, and postoperative feedback. Specific arrangements are coordinated based on the project and region.
  • Patient-specific guides or custom implants typically take 2–4 weeks, with the exact timeline depending on design complexity. For in-stock items, delivery can be arranged within one week.
  • Pricing is determined based on product type, purchase volume, and collaboration model. Agreement support is available for long-term partnerships or bulk procurement.
  • Contact our sales team via Carefix Assistant WhatsApp: +86 18918690107 to receive comprehensive product technical documentation and manuals.
  • Subject to compliance requirements, samples may be requested or clinical evaluations conducted based on project needs.
  • Experienced clinical engineers or product managers can be arranged to provide on-site support based on hospital and surgical requirements.
  • Submit requests via the CareFix official website. We can organize in-person or online technical training sessions and provide standardized surgical guidelines.
  • We regularly participate in orthopedic academic conferences. Users can engage in on-site discussions or virtual meetings to share the latest technologies and clinical experiences.
  • Professional educational materials such as surgical videos, PowerPoint presentations, and clinical case collections can be provided upon request.
  • All medical devices sold in the Chinese market must adhere to national regulations and mandatory standards for production and quality management. They must comply with the Medical Device Production Quality Management Specifications , require operation under the ISO 13485 system, and obtain a Medical Device Registration Certificate to ensure conformity with product technical requirements.
  • In accordance with China's National Medical Products Administration regulations, our Class II and III medical devices implement the UDI system with a "one regulation, one code" management approach. This ensures products are shipped with assigned UDI codes, hospitals scan codes during acceptance, and clinical staff scan codes during use and record the entire process. The UDI code enables upward traceability of production and distribution information and downward traceability of usage impact scope, achieving full traceability throughout the lifecycle.
  • As specified in the product instructions and certificate of conformity, the warranty period varies between sterile and non-sterile conditions.
  • We provide immediate remote support or rapid on-site response through local authorized partners or our headquarters technical support team to ensure surgical safety and continuity.
  • We offer professional testing, refurbishment, and repair services for reusable instruments that comply with quality system requirements, ensuring product performance, safety, and service life meet standards.