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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 10 of 56| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Kinos Aeros Total Ankle Replacement | 1832-0031 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-1034-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-3652-N | FDA UDI | Class II | Active |
| Kinos Instrumentation | 5801-1221 | FDA UDI | Class II | Active |
| restor3d Lumbar Instrument | 5113-L1415 | FDA UDI | Class I | Active |
| restor3d Utility Wedge | 1105-2723120505R | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-4472-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4016-N | FDA UDI | Class II | Active |
| Veritas rTSA | 3500-140C3 | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-1031 | FDA UDI | Class II | Active |
| restor3d Veritas rTSA Instrumentation | 5500-H32U1 | FDA UDI | Class II | Active |
| restor3d Osteotomy Wedge | 1100-002-22140818 | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Wedge Trial | 6101-009-18161218 | FDA UDI | Class I | Active |
| Ossera™ AFX Instrumentation | 6744-5220-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4258-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-5260-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-4072-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-5232-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-1046-N | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 3832-1410 | FDA UDI | Class II | Active |
| restor3d Cervical Cage | 1110-16130807 | FDA UDI | Class II | Active |
| Kinos Axiom | 1801.2140 | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-1035 | FDA UDI | Class II | Active |
| Veritas rTSA | 1500-1145 | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-1067 | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Wedge Trial | 6101-009-20181218 | FDA UDI | Class I | Active |
| Ossera™ AFX Instrumentation | 6740-4060-N | FDA UDI | Class II | Active |
| restor3d Lumbar Instrument | 5113-S1018 | FDA UDI | Class I | Active |
| Ossera™ AFX Instrumentation | 6740-3844-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-4018-N | FDA UDI | Class II | Active |
| restor3d Utility Wedge | 1105-2719101005R | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-4270-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6741-4600-N | FDA UDI | Class II | Active |
| restor3d Cervical Cage | 1110-16131200 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-4252-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-4068-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-1018-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-4056-N | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 3832-1111 | FDA UDI | Class II | Active |
| Kinos Instrumentation | 5801-7414 | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Wedge Trial | 6101-NSP-C0810 | FDA UDI | Class I | Active |
| restor3d Osteotomy Wedge | 1100-001-16140607 | FDA UDI | Class II | Active |
| restor3d Osteotomy Wedge | 1100-002-22141007 | FDA UDI | Class II | Active |
| restor3d Reusable Trial | 5000-0202 | FDA UDI | Class I | Active |
| Ossera™ AFX | 1742-4270-N | FDA UDI | Class II | Active |
| restor3d Reusable Inserter | 5000-0101 | FDA UDI | Class I | Active |
| restor3d Utility Wedge | 1105-2723100505L | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-4672-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-3452-N | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-7210 | FDA UDI | Class II | Active |
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