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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
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- EUDAMED SRN
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- FDA FEI Number
- 3014833750
- DUNS Number
- —
Catalogue (2760)
Page 15 of 56| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ossera™ AFX Instrumentation | 6740-4674-N | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Wedge Inserter | 6100-INSRTRM3 | FDA UDI | Class I | Active |
| Kinos Axiom | 2831.0114 | FDA UDI | Class II | Unknown |
| Ossera™ AFX Instrumentation | 6740-4062-N | FDA UDI | Class II | Active |
| Kinos Aeros Total Ankle Replacement | 1833-0208 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4222-N | FDA UDI | Class II | Active |
| restor3d Cervical Cage | 1110-17150807 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-4668-N | FDA UDI | Class II | Active |
| restor3d Utility Wedge | 1105-2719120005L | FDA UDI | Class II | Active |
| Kinos Axiom | 2831.3005 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4036-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-3674-N | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Wedge Trial | 6100-NSP-A0405 | FDA UDI | Class I | Active |
| restor3d Disposable Instrument, Cervical Cage Trial | 6110-16131007 | FDA UDI | Class I | Active |
| restor3d, Disposable Instrument, Cervical Cage Trial | 6110-001-17151107 | FDA UDI | Class I | Active |
| Kinos Instrumentation | 5801-7013 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-3620-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-3854-N | FDA UDI | Class II | Active |
| Kinos Aeros Instrumentation | 5871-0056 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-3464-N | FDA UDI | Class II | Active |
| restor3d Cervical Cage | 1110-17150500 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-3146-N | FDA UDI | Class II | Active |
| Kinos Axiom | 2831.0214 | FDA UDI | Class II | Unknown |
| Kinos Axiom | 3801-1310 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-3666-N | FDA UDI | Class II | Active |
| Veritas rTSA | 3500-132C3 | FDA UDI | Class II | Active |
| Kinos Instrumentation | 5801-2123 | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Wedge Trial | 6105-2719100005 | FDA UDI | Class I | Active |
| restor3d Cervical Cage | 1110-001-16130707 | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 2833-2002 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-3466-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-3648-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-3666-N | FDA UDI | Class II | Active |
| restor3d Veritas rTSA Instrumentation | 5500-2801 | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 3832-2306 | FDA UDI | Class II | Active |
| restor3d Lumbar Instrument | 5113-M1018 | FDA UDI | Class I | Active |
| Ossera™ AFX | 1744-4152-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4260-N | FDA UDI | Class II | Active |
| restor3d Veritas rTSA Instrumentation | 5500-3603 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-4020-N | FDA UDI | Class II | Active |
| Kinos Instrumentation | 5801-7114 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-3454-N | FDA UDI | Class II | Active |
| restor3d Lumbar Instrument | 5113-S1615 | FDA UDI | Class I | Active |
| Ossera™ AFX Instrumentation | 6743-3450-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-3856-N | FDA UDI | Class II | Active |
| restor3d Lumbar Instrument | 5113-S1412 | FDA UDI | Class I | Active |
| Veritas rTSA | 3500-136U3 | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-1018 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-5158-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-4038-N | FDA UDI | Class II | Active |
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