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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 8 of 56| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ossera™ AFX Instrumentation | 6744-5224-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4474-N | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-1039 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-5214-N | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Cervical Cage Trial | 6110-N01-KTM01 | FDA UDI | Class I | Active |
| restor3d Veritas rTSA Instrumentation | 5500-3605 | FDA UDI | Class II | Active |
| Kinos Instrumentation | 5801-8200 | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Wedge Trial | 6100-002-22140807 | FDA UDI | Class I | Active |
| Ossera™ AFX Instrumentation | 6740-3658-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-4114-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-4648-N | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-1090 | FDA UDI | Class II | Active |
| restor3d Osteotomy Wedge | 1100-16140507 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-4250-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-5242-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-4046-N | FDA UDI | Class II | Active |
| restor3d Utility Wedge | 1105-2723101005L | FDA UDI | Class II | Active |
| restor3d Utility Wedge | 1105-2723121005R | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-4064 | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-0092 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-5150-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-4654-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-4470-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-3620-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-5056-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-3650-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-3422-N | FDA UDI | Class II | Active |
| Kinos Instrumentation | 5801-1213 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-3866-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-4438-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-1056-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-3636-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-5160-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-3158-N | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 3832-1213 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4672-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-5274-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-3418-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-3870-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-3440-N | FDA UDI | Class II | Active |
| restor3d Lumbar Instrument | 5113-S1418 | FDA UDI | Class I | Active |
| Kinos Total Ankle Replacement | 3832-2110 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-3650-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4468-N | FDA UDI | Class II | Active |
| restor3d Reverse Total Shoulder Instrumentation | 6500-2707-N | FDA UDI | Class I | Active |
| Ossera™ AFX Instrumentation | 6742-3842-N | FDA UDI | Class II | Active |
| Kinos Aeros Instrumentation | 5871-9818 | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 3832-1310 | FDA UDI | Class II | Active |
| Kinos Instrumentation | 5801-7006 | FDA UDI | Class II | Active |
| restor3d Lumbar Implant | 1113-S1212 | FDA UDI | Class II | Active |
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