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Sign in to claim this brandAuxano Medical LLC
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 8006 Katherine Boulevard, Brecksville, OH, 44141
- Website
- auxanomedical.net
- —
- —
- [email protected]
- Phone
- 4402622000
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3030271054
- DUNS Number
- 119185571
Catalogue (63)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| INTREPED, Intraosseous Fusion Device | 01-10615 | FDA UDI | Class II | Active |
| INTREPED, Intraosseous Fusion Device | 01-11014 | FDA UDI | Class II | Active |
| INTREPED, Intraosseous Fusion Device | 01-10915 | FDA UDI | Class II | Active |
| INTREPED, Intraosseous Fusion Device | 01-40710 | FDA UDI | Class II | Active |
| INTREPED, Intraosseous Fusion Device | 01-40006 | FDA UDI | Class II | Active |
| INTREPED, Intraosseous Fusion Device | 01-40109 | FDA UDI | Class II | Active |
| INTREPED, Intraosseous Fusion Device | 01-40310 | FDA UDI | Class II | Active |
| INTREPED, Intraosseous Fusion Device | 01-10914 | FDA UDI | Class II | Active |
| INTREPED, Intraosseous Fusion Device | 01-10912 | FDA UDI | Class II | Active |
| INTREPED, Intraosseous Fusion Device | 01-70005 | FDA UDI | Class II | Active |
| INTREPED, Intraosseous Fusion Device | 01-40610 | FDA UDI | Class II | Active |
| Intraosseous Fusion Device System | K231649 | FDA 510(k) | Class II | Active |
| Auxano® Wedge Fixation System | K251791 | FDA 510(k) | Class II | Active |
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