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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 49 of 56| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ossera™ AFX Instrumentation | 6744-1038-N | FDA UDI | Class II | Active |
| restor3d Utility Wedge | 1105-2723140005R | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Cervical Cage Trial | 6110-17150800 | FDA UDI | Class I | Active |
| Ossera™ AFX | 1743-4672-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4472-N | FDA UDI | Class II | Active |
| restor3d Lumbar Instrument | 5113-S0812 | FDA UDI | Class I | Active |
| Kinos Total Ankle Replacement | 3832-1106 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-2068-N | FDA UDI | Class II | Active |
| Veritas rTSA | 1506-1004 | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-0020 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-3022-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-3836-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-5022-N | FDA UDI | Class II | Active |
| Veritas rTSA | 1501-4004 | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-7106 | FDA UDI | Class II | Active |
| Veritas rTSA | 1506-1001 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4442-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-4674-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-4246-N | FDA UDI | Class II | Active |
| Kinos Aeros Instrumentation | 5871-9817 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-4166-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-4450-N | FDA UDI | Class II | Active |
| Kinos Instrumentation | 5801-8400 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-4670-N | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 3832-1406 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-4030-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-4268-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-3418-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-4662-N | FDA UDI | Class II | Active |
| restor3d Lumbar Instrument | 5113-A5001 | FDA UDI | Class I | Active |
| Ossera™ AFX Instrumentation | 6743-3674-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6741-3801-N | FDA UDI | Class II | Active |
| Veritas rTSA | 3500-540U3 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-3434-N | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Wedge | 6101-INSERTER-NS | FDA UDI | Class I | Active |
| restor3d Kinos Axiom Total Ankle System | 1831.2150 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-5038-N | FDA UDI | Class II | Active |
| restor3d Utility Wedge | 1105-2719140505R | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-3162-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4270-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-3646-N | FDA UDI | Class II | Active |
| Kinos Instrumentation | 5801-4111 | FDA UDI | Class II | Active |
| restor3d Cervical Cage | 1110-001-17150607 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-4142-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4616-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-4256-N | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Cervical Cage Trial | 6110-001-16130607 | FDA UDI | Class I | Active |
| Ossera™ AFX | 1744-3048-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4620-N | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-4066 | FDA UDI | Class II | Active |
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