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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 30 of 56| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ossera™ AFX | 1742-3456-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-4270-N | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Cervical Cage Trial | 6110-001-14110607 | FDA UDI | Class I | Active |
| Ossera™ AFX Instrumentation | 6744-1028-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-4456-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-3838-N | FDA UDI | Class II | Active |
| restor3d Osteotomy Wedge | 1100-001-20140607 | FDA UDI | Class II | Active |
| restor3d Cervical Cage | 1110-17150707 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-4066-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4070-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-3660-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-4068-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-1018-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-4044-N | FDA UDI | Class II | Active |
| restor3d Lumbar Instrument | 5113-M1412 | FDA UDI | Class I | Active |
| Ossera™ AFX | 1740-3436-N | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 2834-1004 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-5058-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-4038-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-4440-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-4266-N | FDA UDI | Class II | Active |
| restor3d Lumbar Instrumentation | 5113-B7001 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-3840-N | FDA UDI | Class II | Active |
| restor3d Cervical Cage | 1110-14111200 | FDA UDI | Class II | Active |
| restor3d Veritas rTSA Instrumentation | 5500-3201 | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 3832-2107 | FDA UDI | Class II | Active |
| Kinos Axiom | 3801-2210 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-4120-N | FDA UDI | Class II | Active |
| restor3d Lumbar Instrument | 5113-M1015 | FDA UDI | Class I | Active |
| Ossera™ AFX | 1740-3636-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-3864-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-4474-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-5032-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-3160-N | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Cervical Cage Trial | 6110-14110607 | FDA UDI | Class I | Active |
| restor3d Kinos Axiom Total Ankle System | 1831.2151 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-5266-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-4258-N | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 3832-2314 | FDA UDI | Class II | Active |
| restor3d Cervical Cage | 1110-16130800 | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 3832-2216 | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Wedge Trial | 6100-N02-A0708 | FDA UDI | Class I | Active |
| restor3d Cervical Cage | 1110-14111107 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-3470-N | FDA UDI | Class II | Active |
| Kinos Axiom | 3801-2106 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-4656-N | FDA UDI | Class II | Active |
| restor3d Lumbar Implant | 1113-M1612 | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Cervical Cage Trial | 6110-17150900 | FDA UDI | Class I | Active |
| restor3d Veritas rTSA Instrumentation | 5500-2002 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-4648-N | FDA UDI | Class II | Active |
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