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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 39 of 56| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Veritas rTSA | 3500-536U3 | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-1069 | FDA UDI | Class II | Active |
| Kinos Axiom Total Ankle Replacement | 1834-0131 | FDA UDI | Class II | Active |
| Veritas rTSA | 3500-332C1 | FDA UDI | Class II | Active |
| restor3d Veritas rTSA Instrumentation | 5500-3604 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-3148-N | FDA UDI | Class II | Active |
| Kinos Aeros Instrumentation | 5871-4102 | FDA UDI | Class II | Active |
| Kinos Aeros Instrumentation | 5871-4114 | FDA UDI | Class II | Active |
| Kinos Axiom Total Ankle Replacement | 1834-0030 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-4468-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-4434-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-3446-N | FDA UDI | Class II | Active |
| Kinos Axiom | 5801.0005 | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Cervical Cage Trial | 6110-17151107 | FDA UDI | Class I | Active |
| Ossera™ AFX | 1742-4650-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-3814-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-3464-N | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Cervical Cage Trial | 6110-16131107 | FDA UDI | Class I | Active |
| Kinos Total Ankle Replacement | 3832-2213 | FDA UDI | Class II | Active |
| restor3d Cervical Cage | 1110-14111000 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-2018-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-4216-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-2036-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-1048-N | FDA UDI | Class II | Active |
| Kinos Axiom | 3801-1306 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-4670-N | FDA UDI | Class II | Active |
| restor3d Veritas rTSA Instrumentation | 4520-1003 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-3642-N | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 3832-1116 | FDA UDI | Class II | Active |
| restor3d Cervical Cage | 1110-17151207 | FDA UDI | Class II | Active |
| restor3d Cervical Cage | 1110-001-14110607 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4670-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4434-N | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 3832-2215 | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-8412 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-4150-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4426-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-3652-N | FDA UDI | Class II | Active |
| restor3d, Disposable Instrument, Cervical Cage Trial | 6110-001-14110807 | FDA UDI | Class I | Active |
| Kinos Instrumentation | 5801-1120 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-3852-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-3870-N | FDA UDI | Class II | Active |
| Kinos Axiom | 2831.0215 | FDA UDI | Class II | Unknown |
| Ossera™ AFX Instrumentation | 6744-5156-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-3654-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-3428-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-4122-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4068-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-3864-N | FDA UDI | Class II | Active |
| Kinos Axiom | 3801-2510 | FDA UDI | Class II | Active |
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