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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 42 of 56| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ossera™ AFX Instrumentation | 6744-1054-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-3850-N | FDA UDI | Class II | Active |
| Kinos Instrumentation | 5801-1123 | FDA UDI | Class II | Active |
| restor3d Osteotomy Wedge | 1100-001-20140407 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-4242-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-3132-N | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-1040 | FDA UDI | Class II | Active |
| Veritas rTSA | 3500-340C3 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-3844-N | FDA UDI | Class II | Active |
| restor3d Utility Wedge | 1101-010-222210 | FDA UDI | Class II | Active |
| Kinos Instrumentation | 5801-2213 | FDA UDI | Class II | Active |
| restor3d Osteotomy Wedge | 1101-009-18161218 | FDA UDI | Class II | Active |
| Kinos Axiom | 3801-2308 | FDA UDI | Class II | Active |
| Kinos Axiom | 3801-2206 | FDA UDI | Class II | Active |
| Kinos Axiom | 2831-4004 | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-3116 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-5052-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-4444-N | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-1002 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-4470-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-1026-N | FDA UDI | Class II | Active |
| restor3d Utility Wedge | 1105-2719101005L | FDA UDI | Class II | Active |
| Veritas rTSA | 1504-4854 | FDA UDI | Class II | Active |
| restor3d Lumbar Implant | 1113-M1012 | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Cervical Cage Trial | 6110-17150907 | FDA UDI | Class I | Active |
| Ossera™ AFX | 1744-2044-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-3658-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-5054-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-3144-N | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-4105 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-4058-N | FDA UDI | Class II | Active |
| restor3d Kinos Axiom PSR | 5831-9004 | FDA UDI | Class II | Active |
| Kinos Instrumentation | 5801-2223 | FDA UDI | Class II | Active |
| restor3d Lumbar Instrument | 5113-S1012 | FDA UDI | Class I | Active |
| restor3d Lumbar Instrumentation | 5113-B4001 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-5150-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-5218-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-5036-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-2046-N | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Wedge Trial | 6105-2723140005 | FDA UDI | Class I | Active |
| Ossera™ AFX Instrumentation | 6744-3074-N | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-3113 | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-1016 | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Cervical Cage Trial | 6110-17151100 | FDA UDI | Class I | Active |
| Kinos Axiom | 2801.2002 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-3846-N | FDA UDI | Class II | Active |
| Kinos Aeros Total Ankle Replacement | 1832-0040 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-5154-N | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Cervical Cage Trial | 6110-14111007 | FDA UDI | Class I | Active |
| Veritas rTSA | 1506-1007 | FDA UDI | Class II | Active |
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