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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 41 of 56| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ossera™ AFX Instrumentation | 6740-4058-N | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-1022 | FDA UDI | Class II | Active |
| Kinos Axiom | 1801.1120 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-4058-N | FDA UDI | Class II | Active |
| restor3d Osteotomy Wedge | 1101-009-20180818 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-4448-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-5144-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-4462-N | FDA UDI | Class II | Active |
| restor3d Veritas rTSA Instrumentation | 5500-1001 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-4250-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-2042-N | FDA UDI | Class II | Active |
| Veritas rTSA | 3500-336U1 | FDA UDI | Class II | Active |
| Veritas rTSA | 3500-140U1 | FDA UDI | Class II | Active |
| restor3d Veritas rTSA Instrumentation | 5500-1911 | FDA UDI | Class II | Active |
| Kinos Axiom | 5801.0011 | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 2834-2001 | FDA UDI | Class II | Active |
| restor3d Utility Wedge | 1105-2719120005R | FDA UDI | Class II | Active |
| Kinos Aeros Instrumentation | 5871-1158 | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Cervical Cage Inserter | 6110-INSRTRM3 | FDA UDI | Class I | Active |
| restor3d Utility Wedge | 1105-2723100005L | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-4254-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-3850-N | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 3832-2407 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-5134-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-4128-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-2074-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4048-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-5020-N | FDA UDI | Class II | Active |
| restor3d Disposable Instrument | 4110-S014 | FDA UDI | Class I | Active |
| Ossera™ AFX | 1744-3172-N | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Cervical Cage Trial | 6110-N01-KTS01 | FDA UDI | Class I | Active |
| Kinos Instrumentation | 5801-2111 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-4474-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-3444-N | FDA UDI | Class II | Active |
| Kinos Instrumentation | 5801-7314 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-4118-N | FDA UDI | Class II | Active |
| restor3d Lumbar Instrument | 5113-S1218 | FDA UDI | Class I | Active |
| restor3d Reusable Trial | 5000-0302 | FDA UDI | Class I | Active |
| restor3d Osteotomy Wedge | 1101-22200818 | FDA UDI | Class II | Active |
| restor3d MTP | 1103-161420 | FDA UDI | Class II | Active |
| restor3d Osteotomy Wedge | 1100-20140507 | FDA UDI | Class II | Active |
| Kinos Instrumentation | 5801-1211 | FDA UDI | Class II | Active |
| restor3d Utility Wedge | 1105-2723141005L | FDA UDI | Class II | Active |
| restor3d, Disposable Instrument, Cervical Cage Trial | 6110-001-17150807 | FDA UDI | Class I | Active |
| Ossera™ AFX | 1744-5220-N | FDA UDI | Class II | Active |
| restor3d Cervical Cage | 1110-17150600 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4242-N | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Cervical Cage Trial | 6110-16130600 | FDA UDI | Class I | Active |
| Kinos Axiom | 3801.1106 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-3838-N | FDA UDI | Class II | Active |
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