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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
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3014833750
- DUNS Number
- —
Catalogue (2760)
Page 34 of 56| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Kinos Axiom | 3801-1212 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-3634-N | FDA UDI | Class II | Active |
| Kinos Axiom | 5801.4109 | FDA UDI | Class I | Unknown |
| Kinos Axiom Instrumentation | 5801-7206 | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-1079 | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-7408 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1741-3400-N | FDA UDI | Class II | Active |
| Kinos Axiom | 2801.1005 | FDA UDI | Class II | Unknown |
| restor3d Disposable Instrument Kit | 4110-S011 | FDA UDI | Class I | Active |
| Kinos Axiom Instrumentation | 5801-1078 | FDA UDI | Class II | Active |
| Veritas rTSA | 3500-136C3 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-3462-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-3462-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-3430-N | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 3832-2114 | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Wedge | 6101-INSERTER | FDA UDI | Class I | Active |
| Ossera™ AFX | 1744-2054-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-3464-N | FDA UDI | Class II | Active |
| Veritas rTSA | 1501-3608 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-4074-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-4264-N | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-4032 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4018-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-4274-N | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Wedge Trial | 6101-NSP-A1012 | FDA UDI | Class I | Active |
| Ossera™ AFX | 1744-3154-N | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Cervical Cage Trial | 6110-14110500 | FDA UDI | Class I | Active |
| restor3d, Disposable Instrument, Cervical Cage Trial | 6110-001-17151007 | FDA UDI | Class I | Active |
| Ossera™ AFX Instrumentation | 6740-4254-N | FDA UDI | Class II | Active |
| Veritas rTSA | 1501-3208 | FDA UDI | Class II | Active |
| Kinos Instrumentation | 5801-2210 | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Wedge Trial | 6101-22201218 | FDA UDI | Class I | Active |
| Ossera™ AFX | 1743-4258-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-3826-N | FDA UDI | Class II | Active |
| Kinos Axiom | 3801-2506 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-3064-N | FDA UDI | Class II | Active |
| restor3d Cervical Cage | 1110-17150607 | FDA UDI | Class II | Active |
| Veritas rTSA | 1505-4818 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-4048-N | FDA UDI | Class II | Active |
| restor3d Lumbar Instrumentation | 5113-B7002 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-1068-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-3668-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-3032-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-4264-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-3046-N | FDA UDI | Class II | Active |
| Kinos Instrumentation | 5871-2724 | FDA UDI | Class II | Active |
| Kinos Axiom Total Ankle Replacement | 1834-0052 | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Cervical Cage Trial | 6110-16130607 | FDA UDI | Class I | Active |
| restor3d Disposable Instrument, Cervical Cage Trial | 6110-16130500 | FDA UDI | Class I | Active |
| Kinos Axiom | 2831-4001 | FDA UDI | Class II | Active |
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