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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 29 of 56| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ossera™ AFX | 1744-2030-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-5064-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-3472-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-2042-N | FDA UDI | Class II | Active |
| Kinos Axiom | 3801-2112 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-4038-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-3650-N | FDA UDI | Class II | Active |
| restor3d Lumbar Instrumentation | 5113-B5021 | FDA UDI | Class II | Active |
| Veritas rTSA | 3500-540C1 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-5170-N | FDA UDI | Class II | Active |
| Kinos Aeros Instrumentation | 5871-9819 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-4074-N | FDA UDI | Class II | Active |
| restor3d Utility Wedge | 1105-2719100005L | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-4038-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-5042-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-4456-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-3670-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-3452-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-3460-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-3456-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-3846-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-4066-N | FDA UDI | Class II | Active |
| Kinos Total Ankle Instrumentation | 5801-4072 | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 3832-1214 | FDA UDI | Class II | Active |
| Kinos Axiom | 2801.2003 | FDA UDI | Class II | Active |
| restor3d Veritas rTSA Instrumentation | 5500-2802 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-3628-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-1040-N | FDA UDI | Class II | Active |
| restor3d Cervical Cage | 1110-14110707 | FDA UDI | Class II | Active |
| restor3d Cervical Cage | 1110-001-17150707 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-3420-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4228-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-3474-N | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 3832-2311 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-3838-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-2064-N | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Cervical Cage Trial | 6110-001-16130507 | FDA UDI | Class I | Active |
| Ossera™ AFX | 1744-4136-N | FDA UDI | Class II | Active |
| restor3d Disposable Trial Kit | 4100-0101 | FDA UDI | Class I | Unknown |
| Ossera™ AFX Instrumentation | 6744-4162-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-1074-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-3466-N | FDA UDI | Class II | Active |
| Veritas rTSA | 1500-1130 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-4036-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-3632-N | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Wedge Trial | 6105-2723141005 | FDA UDI | Class I | Active |
| restor3d Osteotomy Wedge | 1101-009-20181018 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-4246-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-4646-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-4458-N | FDA UDI | Class II | Active |
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