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A XC Medico is an ISO 13485:2016 certified manufacturer. Our external fixation devices hold CE certification and are registered with FDA (Class I/II) where applicable. Please ask our team for specific certificate documents.
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A Generally, our external fixator sets and instruments are supplied non-sterile and must be sterilized by the hospital (autoclave) before use. However, sterile packaging options are available upon request for specific orders.
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A Yes, our Modular External Fixation System is designed with universal compatibility in mind. Our connecting rods and clamps can often be used interchangeably with mainstream international systems, offering flexibility for surgeons.
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A Our systems are manufactured using medical-grade Titanium Alloy , Stainless Steel , and high-strength Carbon Fiber (for radiolucent connecting rods). All materials are biocompatible and meet ISO standards.
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A Please contact our sales team via the form below or WhatsApp. To receive an accurate quote, please specify the Product Series (e.g., Ilizarov, Monolateral), Material preference (Titanium/SS/Carbon Fiber), and Quantity . We usually respond within 24 hours.
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A To support new partners, we offer a flexible MOQ. You can order as low as one set (instrument box + implants) to start. We are committed to growing with our distributors.
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A For standard stock items (e.g., Mono-lateral frames, Schanz screws), we ship within 72 hours . For customized orders or large-scale OEM production, the lead time is typically 15 days . Global transit time varies (7-15 business days) based on air/sea freight options.
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A Absolutely. We encourage distributors to request sample kits to evaluate our material quality and locking mechanisms. Sample preparation usually takes 3-5 days depending on the specifications (e.g., Titanium or Carbon Fiber components).
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A Yes, we specialize in OEM/ODM solutions . We can customize external fixators according to your clinical requirements, including private labeling (laser marking) , custom instrument kit configurations, and packaging design to fit your local market needs.
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A Quality is our priority. XC Medico offers a 1-year warranty on all external fixation systems covering manufacturing defects and material fatigue. Every fixator and instrument set undergoes 100% rigorous testing in our mechanics laboratory before shipment.
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A XC Medico operates under a strict medical-grade quality management system. We are ISO 13485 certified , and our products comply with CE and major international regulatory standards, ensuring 100% traceability and safety.
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A Absolutely. We offer complete, high-precision surgical instrument sets for all our spinal systems (Open, MIS, Cervical, etc.). Our instruments are ergonomically designed for surgeon comfort and are fully compatible with our implants to ensure smooth intraoperative procedures.
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A We refuse to compromise on quality. Our titanium implants are manufactured from premium Ti6Al4V ELI (Grade 23) sourced from trusted global suppliers. Our PEEK cages use certified material (e.g., from Invibio or equivalent medical-grade sources), ensuring biocompatibility and mechanical strength comparable to top international brands.
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A For in-stock items, we can ship within 3-7 days thanks to our efficient inventory management (and regional warehousing options). For customized or large-volume production orders, the standard lead time is typically 2-4 weeks, significantly faster than the industry average.
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A We offer a flexible MOQ policy to support your business growth. For standard products, we accept small trial orders. For customized OEM orders, the MOQ is negotiated based on complexity, but we strive to keep it friendly for startups and established distributors alike.
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A Yes, we specialize in comprehensive OEM/ODM solutions. We offer laser marking for your logo, custom packaging design, and can even develop private molds based on your specific drawings or samples to help build your brand.
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A To ensure safety and compliance, sports medicine implants should be certified with international standards such as FDA (USA), CE Mark (Europe), and ISO 13485 (quality management systems). These certifications demonstrate regulatory approval and product reliability.
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A Surgeons consider factors like injury type, patient activity level, bone quality, implant material, and surgical approach. They often rely on clinical experience and current research to select optimal fixation devices for ACL, meniscus, or shoulder repair.
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A Minimally invasive arthroscopy reduces surgical trauma, shortens recovery time, lowers infection risk, and offers excellent joint visualization. It has become the standard approach for diagnosing and treating sports-related joint injuries.
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A 3D printing enables rapid prototyping and precise customization of implants and surgical guides. It allows orthopedic companies to create patient-specific tools, match anatomical variations, and test biomechanical performance before production.