Axiora Medical
Axiora Medical
Highly precise tools and components designed for initial interventions and complex joint reconstruction in Riyadh's leading orthopedic centers.
Riyadh is at the epicentre of a major healthcare revolution driven by Saudi Arabia's Vision 2030 program. With the rapid expansion of specialized orthopedic units in prestigious medical destinations like King Faisal Specialist Hospital, National Guard Health Affairs (NGHA), and King Khalid University Hospital, the demand for high-end hip and knee reconstruction implants has reached unprecedented levels.
Our THR and TKR portfolios are designed specifically to support clinical professionals in Riyadh. Engineered from premium medical-grade Titanium Alloy (Ti6Al4V) and Cobalt-Chromium-Molybdenum (CoCrMo), our implants deliver exceptional wear resistance, optimized load transfer, and robust secondary stabilization for patients undergoing primary or revision arthroplasty.
Our engineering processes align with SFDA Class III requirements, ensuring registration pathways for our Riyadh supply partners are clear of bureaucratic friction.
With an increase in active aging demographics in Saudi Arabia, our dual-mobility hip cups and cruciate-substituting knee joints withstand high mechanical stresses.
Providing customized branding, custom packaging, and specific anatomical size scales matching the Middle Eastern morphometric profiles.
Engineered to support precise physiological alignment, biological fixation, and minimal wear properties.
Delivering high clinical-grade implants validated by comprehensive testing and ISO 13485 cleanroom manufacturing standards.
Our implants utilize Plasma Sprayed Titanium coating and Hydroxyapatite (HA) coating interfaces to facilitate fast and stable biological fixation. This dual-coating methodology replicates natural bone density structures, significantly minimizing the risk of aseptic loosening, which is historically a primary cause of early-stage revision surgery.
Every batch of femoral stems, acetabular cups, and tibial base plates undergoes rigid geometric and mechanical stress testing. Our internal QA department consists of 48 dedicated quality control inspectors utilizing Coordinate Measuring Machines (CMM), dynamic fatigue testing rigs, and surface roughness interferometers to guarantee adherence to ISO 5832 specifications.
| Biomechanical Feature | Manufacturing Specification | Clinical Value |
|---|---|---|
| Stem Substrate | ASTM F136 Ti6Al4V ELI Alloy | Exceptional Fatigue Strength & Biocompatibility |
| Coating Roughness | Ra 30 - 50 μm (Plasma Sprayed) | Accelerated Secondary Bone Ingrowth |
| UHMWPE Polyethylene | Highly Cross-linked (XLPE) + Vitamin E | Prevents Long-term Delamination & Oxidation |
| Taper Dimensions | 12/14 Taper System Standard | Universal Component Compatibility |
| Wear Interface | CoCrMo or Alumina Ceramic on XLPE | Minimized Osteolysis Rates in Active Patients |
A globally recognized manufacturer delivering ISO 13485-certified trauma, joint reconstruction, and spinal systems.
Axiora Medical Technology (China) Co., Ltd. is a professional manufacturer specializing in the research, development, production, and global supply of high-quality orthopedic implants and surgical instruments. Our product portfolio covers trauma fixation systems, spinal implants, joint reconstruction solutions, sports medicine products, and related orthopedic surgical instruments.
Established with a commitment to innovation and precision manufacturing, Axiora integrates advanced CNC machining, automated production lines, and strict quality management systems to deliver reliable products that meet international standards. Our experienced engineering team continuously develops innovative solutions to support surgeons and healthcare providers worldwide.
With strong OEM and ODM capabilities, we provide customized manufacturing services according to customers' drawings, samples, and technical requirements. From product design and prototyping to mass production and packaging, our integrated manufacturing process ensures consistent quality, competitive pricing, and on-time delivery.
Today, Axiora exports its orthopedic products to customers across Europe, North America, South America, the Middle East, Southeast Asia, and Africa, building long-term partnerships with medical device distributors, brand owners, hospitals, and healthcare organizations around the world.
| Axiora Operations & Quality Infrastructure Details | |
|---|---|
| Brand | Axiora |
| Established Year | 2017 |
| Factory Area | 18,600 m² |
| Export Experience | 8 Years |
| Quality Inspection | 100% Finished Product Inspection & Incoming Material Inspection |
| Inspection Infrastructure | Coordinate Measuring Machine (CMM), Tensile Testing, Hardness Testing, Surface Roughness Inspection, Salt Spray Testing |
| Supply Chain Partners | 1,120 Globally |
| Customization Capabilities | Logo Printing, Private Label, Custom Packaging, Product Design, Material Selection, Drawing-Based Manufacturing |
| R&D Output | 126 New Products Released Last Year |
Inside our ISO-Class 7 cleanrooms and high-precision CNC multi-axis fabrication facility.
Simulating 5+ years of clinical deployment to assure long-term stabilization parameters in extreme dry and humid climates.
Streamlining lead times, regulatory documentation, and logistical pathways to the Riyadh Province.
We provide comprehensive documentation support including ISO 13485 design dossiers, biocompatibility protocols, and CE Class III certification templates to expedite approval through the Saudi Food and Drug Authority (SFDA).
We offer fully customized, pre-sterilized primary packaging featuring local Arabic-English regulatory barcodes, custom product nomenclature, and private labels matching regional hospital procurement demands.
Express air cargo shipments directly to King Khalid International Airport (RUH) with full customs documentation, certificate of origin validation by the chamber of commerce, and reliable cold-chain protection.
Premium implants and instrument sets configured for optimal clinical outcomes in primary and revision cases.
Technical and regulatory answers regarding the supply of THR/TKR systems in Riyadh.
Yes. We have a dedicated regulatory affairs division that provides the complete technical dossiers (including biomechanical test data, clinical evaluation records, and ISO 13485 certificates) required to register Class III medical devices with the SFDA in Saudi Arabia. We partner with local distributors in Riyadh to smooth the submission process.
We use industry-standard biocompatible raw materials sourced from certified international suppliers. Stems and cups are produced from Titanium Alloy (Ti-6Al-4V ELI conforming to ASTM F136 / ISO 5832-3). Our femoral heads and knee components are manufactured from Cobalt-Chromium-Molybdenum (CoCrMo conforming to ISO 5832-12). Bearing surfaces are made of Highly Cross-linked Polyethylene (XLPE) or BIOLOX Delta compatible ceramics.
All implants are processed in our certified Class 10,000 (ISO Class 7) cleanrooms. Standard packages are double-sterile blister packs sterilized via Ethylene Oxide (EO) or Gamma irradiation. The packaging includes high-barrier protective seals to ensure sterility is maintained during long-distance maritime or air transit to storage facilities in Riyadh.
For standard configurations, the production cycle ranges from 30 to 45 days depending on the volume. Custom OEM/ODM modifications (such as specific surface treatment variations or customized surgical instrument sets) typically require 60 to 90 days from technical drawing sign-off to final quality release.
Yes. Our joint instrument portfolios (such as our Hip Revision Instrument Set and T-Handle Extractor Set) can be customized. We can modify tray layouts, include custom logo markings on instruments via laser etching, and provide tailored surgical tool configurations based on input from your clinical advisors.
