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Sign in to claim this brandKinamed, Inc.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 820 Flynn Rd, CAMARILLO, CA, 93012
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 2027148
- DUNS Number
- 184896645
Catalogue (346)
Page 7 of 7| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| KineMatch® PFR System | 22-800-3004 | FDA UDI | Class I | Unknown |
| CarboJet XF® Bone Preparation System | 27-100-1000 | FDA UDI | Class II | Active |
| MD3T™ Multi-Directional Tibial Tubercle Transfer System | 23-800-2001 | FDA UDI | Class I | Active |
| KineMatch® PFR System | Custom 102 | FDA UDI | Class II | Active |
| KineMatch® PFR System | 22-800-2001 | FDA UDI | Class I | Active |
| KineMatch® PFR System | Custom 106 | FDA UDI | Class I | Active |
| KineMatch® PFR System | 22-800-4001 | FDA UDI | Class I | Active |
| CarboJet® CO2 Bone Lavage System | 25-200-0244 | FDA UDI | Class II | Active |
| KineMatch® PFR System | 22-800-3020 | FDA UDI | Class I | Active |
| CarboJet® CO2 Bone Lavage System | 25-200-0110 | FDA UDI | Class II | Active |
| KineMatch® PFR System | 22-800-3023 | FDA UDI | Class I | Active |
| CarboJet® CO2 Bone Lavage System | 25-200-0250 | FDA UDI | Class II | Active |
| CarboJet® CO2 Bone Lavage System | 25-200-0162 | FDA UDI | Class II | Active |
| Orthopilot | K003347 | FDA 510(k) | Class II | Active |
| Kinamed 32mm Bioceram-Z Toatal Hip Femoral Ball | K920290 | FDA 510(k) | Class II | Active |
| Acetabular Shells & Liners For Ath Total Hip Syst. | K893821 | FDA 510(k) | Class II | Active |
| Cth Stabilo Total Hip Replacement System | K903976 | FDA 510(k) | Class II | Active |
| Reality Long Stem Hip System | K954219 | FDA 510(k) | Class II | Active |
| Kinamed Ath-Porous And Ath-Porous Long Total Hip | K922421 | FDA 510(k) | Class II | Active |
| Gem Posterior Stabilized Total Knee System | K010101 | FDA 510(k) | Class II | Active |
| Gem Inset Patellar Component | K032950 | FDA 510(k) | Class II | Active |
| Supercable Grip And Plate System | K072250 | FDA 510(k) | Class II | Active |
| Gem Knee System | K994214 | FDA 510(k) | Class II | Active |
| Kinamed Reality Total Hip System | K922247 | FDA 510(k) | Class II | Active |
| Iso-Elastic Cerclage System | K030256 | FDA 510(k) | Class II | Active |
| Neuropro Low Profile Cranial Plating System | K122049 | FDA 510(k) | Class II | Active |
| Kinamed Cemented Ath-Long Stem | K902073 | FDA 510(k) | Class II | Active |
| Navipro Shoulder Software Module | K050897 | FDA 510(k) | Class II | Active |
| Kinamed Ath 26mm Cocr Total Hip Femoral Head | K903884 | FDA 510(k) | Class II | Active |
| Kinamed Cemented Cth Stem | K902074 | FDA 510(k) | Class II | Active |
| Kinamed Ceramic Ath Total Hip - 28mm Ball | K894904 | FDA 510(k) | Class II | Active |
| Kinamed Ath 28mm Alumina Ceramic Long-Neck Ball | K912295 | FDA 510(k) | Class II | Active |
| Kinamed 28mm Bioceram-Z Total Hip Femoral Ball | K915310 | FDA 510(k) | Class II | Active |
| Kinematch Patello-Femoral Resurfacing Impalant | K013982 | FDA 510(k) | Class II | Active |
| Kinamed 26mm Bioceran-Z Total Hip Femoral Ball | K920219 | FDA 510(k) | Class II | Active |
| Kinamed Ath 22mm Cocr Total Hlip Femoral Head | K903885 | FDA 510(k) | Class II | Active |
| Ath Ceramic Uhmwpe Total Hip System | K890472 | FDA 510(k) | Class II | Active |
| Kinamed Ctn Stem | K914237 | FDA 510(k) | Class II | Active |
| Ath Full Profile Acetabular Cup System | K954213 | FDA 510(k) | Class II | Active |
| Ath Metal:uhmwpe Total Hip System | K882675 | FDA 510(k) | Class III | Active |
| Kinamed 22mm Bioceram-Z Total Hip Femoral Ball | K915309 | FDA 510(k) | Class II | Active |
| Quick Tap Self Drilling Screw | K982927 | FDA 510(k) | Class II | Active |
| Kinamed Profix System | K964362 | FDA 510(k) | Class II | Active |
| Kinamed Ath-Ha & Ath-Ha Long Total Hip | K914843 | FDA 510(k) | Class II | Active |
| Navipro Knee Software Module | K033668 | FDA 510(k) | Class II | Active |
| Navipro | K020764 | FDA 510(k) | Class II | Active |
Related Companies
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FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Aug 18, 2010 | Z-2588-2011 | — | terminated | The recall was initiated due to inadequate mechanical strength of these screwdrivers' hexagonal tip feature, causing it to strip during final tightening. |