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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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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3014833750
- DUNS Number
- —
Catalogue (2760)
Page 25 of 56| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ossera™ AFX Instrumentation | 6740-3828-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-4450-N | FDA UDI | Class II | Active |
| Kinos Instrumentation | 5801-8100 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-4242-N | FDA UDI | Class II | Active |
| Kinos Aeros Instrumentation | 5871-4061 | FDA UDI | Class II | Active |
| Kinos Axiom | 3801-1408 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4234-N | FDA UDI | Class II | Active |
| Kinos Axiom | 2831-3004 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-5228-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-3874-N | FDA UDI | Class II | Active |
| restor3d Lumbar Implant | 1113-S1018 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-4650-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-3662-N | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-9812 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-5264-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-5134-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-3642-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-1054-N | FDA UDI | Class II | Active |
| Veritas rTSA | 3500-132C1 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-5118-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-1024-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4466-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-2024-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-5234-N | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 3832-2206 | FDA UDI | Class II | Active |
| restor3d Cervical Cage | 1110-001-14110707 | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Wedge Trial | 6100-16140607 | FDA UDI | Class I | Active |
| Kinos Instrumentation | 5801-2112 | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Cervical Cage Trial | 6110-17150700 | FDA UDI | Class I | Active |
| Ossera™ AFX Instrumentation | 6740-4252-N | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-8408 | FDA UDI | Class II | Active |
| Kinos Aeros Instrumentation | 5871-4116 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-3118-N | FDA UDI | Class II | Active |
| Kinos Axiom Total Ankle Replacement | 2832-2001 | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Cervical Cage Trial | 6110-16131100 | FDA UDI | Class I | Active |
| restor3d Osteotomy Wedge | 1100-16140407 | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Wedge Trial | 6101-18161018 | FDA UDI | Class I | Active |
| restor3d Cervical Cage | 1110-14110900 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-3156-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-1030-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-3854-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-4056-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-4258-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-4060-N | FDA UDI | Class II | Active |
| restor3d Veritas rTSA Instrumentation | 5500-2904 | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Wedge Trial | 6101-NSP-A0810 | FDA UDI | Class I | Active |
| Ossera™ AFX Instrumentation | 6744-3032-N | FDA UDI | Class II | Active |
| Kinos Instrumentation | 5801-1113 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-3870-N | FDA UDI | Class II | Active |
| Kinos Axiom | 3801-1510 | FDA UDI | Class II | Active |
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