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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 26 of 56| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ossera™ AFX | 1743-3470-N | FDA UDI | Class II | Active |
| restor3d Kinos Axiom PSR | 5831-9002 | FDA UDI | Class II | Unknown |
| restor3d Cervical Cage | 1110-001-17150807 | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Cervical Cage Trial | 6110-001-17150607 | FDA UDI | Class I | Active |
| Ossera™ AFX Instrumentation | 6740-4648-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-4056-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-4250-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-4062-N | FDA UDI | Class II | Active |
| Kinos Aeros Instrumentation | 5871-1157 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-2032-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-3664-N | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-1021 | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Cervical Cage Trial | 6110-N01-KTL01NST | FDA UDI | Class I | Active |
| Ossera™ AFX Instrumentation | 6743-4264-N | FDA UDI | Class II | Active |
| restor3d Disposable Instrument Kit | 4110-S013 | FDA UDI | Class I | Active |
| Ossera™ AFX Instrumentation | 6742-3472-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-3672-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-4220-N | FDA UDI | Class II | Active |
| Kinos Instrumentation | 5801-7214 | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Wedge Trial | 6100-20140607 | FDA UDI | Class I | Active |
| restor3d, Disposable Instrument, Cervical Cage Trial | 6110-001-16130907 | FDA UDI | Class I | Active |
| Ossera™ AFX Instrumentation | 6740-3466-N | FDA UDI | Class II | Active |
| restor3d Veritas rTSA Instrumentation | 5500-1101 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-3626-N | FDA UDI | Class II | Active |
| restor3d Lumbar Implant | 1113-S1412 | FDA UDI | Class II | Active |
| restor3d Lumbar Instrumentation | 5113-B3011 | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-8406 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4636-N | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 2833-2003 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4626-N | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Cervical Cage Trial | 6110-17150507 | FDA UDI | Class I | Active |
| restor3d Utility Wedge | 1101-010-202010 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-3472-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-4272-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-3666-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-3030-N | FDA UDI | Class II | Active |
| Veritas rTSA | 1504-4826 | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-0047 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-3454-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4224-N | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-1033 | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-1068 | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Wedge Trial | 6100-002-22140907 | FDA UDI | Class I | Active |
| Ossera™ AFX Instrumentation | 6744-3062-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-4474-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-4442-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-4032-N | FDA UDI | Class II | Active |
| restor3d Lumbar Implant | 1113-S1615 | FDA UDI | Class II | Active |
| Veritas rTSA | 1505-4854 | FDA UDI | Class II | Active |
| Kinos Aeros Total Ankle Replacement | 1832-0041 | FDA UDI | Class II | Active |
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