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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 44 of 56| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ossera™ AFX Instrumentation | 6744-2060-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-5048-N | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-1046 | FDA UDI | Class II | Active |
| restor3d Lumbar Implant | 1113-L1018 | FDA UDI | Class II | Active |
| Kinos Axiom | 2831-3001 | FDA UDI | Class II | Active |
| restor3d Osteotomy Wedge | 1101-20181218 | FDA UDI | Class II | Active |
| Veritas rTSA | 3500-536C1 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-4470-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-3434-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-3446-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-4672-N | FDA UDI | Class II | Active |
| restor3d Lumbar Instrument | 5113-M1215 | FDA UDI | Class I | Active |
| Ossera™ AFX | 1740-4040-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-5018-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-3666-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-4244-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-2026-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-5236-N | FDA UDI | Class II | Active |
| Kinos Axiom | 3801-2208 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-3462-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-4670-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-3444-N | FDA UDI | Class II | Active |
| restor3d Lumbar Implant | 1113-M1618 | FDA UDI | Class II | Active |
| Kinos Axiom Total Ankle Replacement | 1834-0120 | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Wedge Trial | 6101-009-20181018 | FDA UDI | Class I | Active |
| Ossera™ AFX | 1740-3838-N | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-9816 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-4452-N | FDA UDI | Class II | Active |
| Veritas rTSA | 1506-1003 | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Wedge Trial | 6105-2723100005 | FDA UDI | Class I | Active |
| Ossera™ AFX | 1744-1044-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-3662-N | FDA UDI | Class II | Active |
| restor3d Cervical Cage | 1110-16130507 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-3872-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-3870-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-5258-N | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-1044 | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 3832-1409 | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 2833-2000 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-4024-N | FDA UDI | Class II | Active |
| restor3d Lumbar Implant | 1113-M1218 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-3864-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-5262-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-5132-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-4042-N | FDA UDI | Class II | Active |
| Kinos Axiom | 1801.1150 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-3168-N | FDA UDI | Class II | Active |
| restor3d Veritas rTSA Instrumentation | 5500-1901 | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Cervical Cage Trial | 6110-001-17150507 | FDA UDI | Class I | Active |
| Ossera™ AFX Instrumentation | 6740-3470-N | FDA UDI | Class II | Active |
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