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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 46 of 56| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ossera™ AFX | 1742-4256-N | FDA UDI | Class II | Active |
| Kinos Axiom | 1801.2110 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-5066-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4052-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-5138-N | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-4107 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-2038-N | FDA UDI | Class II | Active |
| restor3d Cervical Cage | 1110-17151107 | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-4085 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-5244-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-4418-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-5234-N | FDA UDI | Class II | Active |
| restor3d Lumbar Implant | 1113-S1012 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-4014-N | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Cervical Cage Trial | 6110-N01-KTL01 | FDA UDI | Class I | Active |
| Ossera™ AFX Instrumentation | 6744-5142-N | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 3832-1312 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-1024-N | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-1053 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-4464-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4654-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-3460-N | FDA UDI | Class II | Active |
| restor3d Kinos Axiom Total Ankle System | 1831.1150 | FDA UDI | Class II | Active |
| restor3d Cervical Cage | 1110-001-14110907 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-5014-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-4038-N | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 3832-2316 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6741-4000-N | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-4087 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-3458-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-4654-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6741-4401-N | FDA UDI | Class II | Active |
| restor3d Veritas rTSA Instrumentation | 5500-3607 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4664-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-4456-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-3468-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-3838-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-4042-N | FDA UDI | Class II | Active |
| restor3d Kinos Axiom PSR | 5831-9003 | FDA UDI | Class II | Active |
| Kinos Instrumentation | 5801-7016 | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-9108 | FDA UDI | Class II | Active |
| Veritas rTSA | 1501-3601 | FDA UDI | Class II | Active |
| restor3d Lumbar Instrument | 5113-A1003 | FDA UDI | Class I | Active |
| Kinos Axiom Instrumentation | 5801-2071 | FDA UDI | Class II | Active |
| Kinos Axiom | 1801.1131 | FDA UDI | Class II | Active |
| Veritas rTSA | 1501-4008 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-3862-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-4062-N | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-1001 | FDA UDI | Class II | Active |
| restor3d Lumbar Implant | 1113-L1415 | FDA UDI | Class II | Active |
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