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Sign in to claim this brandRestor3D
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 4001 NC Hwy 54, Suite 2160, Durham, NC, 27709
- Website
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- —
- —
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3014833750
- DUNS Number
- —
Catalogue (2760)
Page 22 of 56| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ossera™ AFX | 1743-4068-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-3856-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-3668-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-3672-N | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-8110 | FDA UDI | Class II | Active |
| Kinos Axiom | 5801.0001 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-3026-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1741-4200-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-3166-N | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Wedge Trial | 6101-NSP-B0810 | FDA UDI | Class I | Active |
| Ossera™ AFX | 1744-5126-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-3440-N | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-0052 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-4066-N | FDA UDI | Class II | Active |
| restor3d Veritas rTSA Instrumentation | 4510-1001 | FDA UDI | Class II | Active |
| restor3d Kinos Axiom Total Ankle System | 1831.2141 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-4442-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4622-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-2054-N | FDA UDI | Class II | Active |
| restor3d Lumbar Instrument | 5113-A0001 | FDA UDI | Class I | Active |
| Ossera™ AFX | 1742-4262-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-3134-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-5020-N | FDA UDI | Class II | Active |
| Kinos Axiom | 3801-2310 | FDA UDI | Class II | Active |
| Kinos Instrumentation | 5801-1070 | FDA UDI | Class II | Active |
| restor3d Utility Wedge | 1105-2719140005L | FDA UDI | Class II | Active |
| restor3d Lumbar Implant | 1113-S1218 | FDA UDI | Class II | Active |
| restor3d Lumbar Instrumentation | 5113-B3001 | FDA UDI | Class II | Active |
| restor3d Lumbar Instrumentation | 5113-B2001 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-5116-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-3468-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-2038-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-5050-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-3020-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-4244-N | FDA UDI | Class II | Active |
| Kinos Aeros Total Ankle Replacement | 5871-1060 | FDA UDI | Class II | Active |
| restor3d Disposable Instrument | 6203-1001 | FDA UDI | Class I | Active |
| restor3d Disposable Instrument, Cervical Cage Trial | 6110-17150500 | FDA UDI | Class I | Active |
| restor3d, Disposable Instrument, Cervical Cage Trial | 6110-001-16131107 | FDA UDI | Class I | Active |
| Kinos Axiom Instrumentation | 5801-9212 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-4048-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4428-N | FDA UDI | Class II | Active |
| restor3d Cervical Cage | 1110-14110907 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4630-N | FDA UDI | Class II | Active |
| restor3d Lumbar Instrument | 5113-L1018 | FDA UDI | Class I | Active |
| Ossera™ AFX Instrumentation | 6743-4446-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-1052-N | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Wedge Trial | 6101-NSP-B1012 | FDA UDI | Class I | Active |
| restor3d Cervical Cage | 1110-001-14111107 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-3642-N | FDA UDI | Class II | Active |
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