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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 11 of 56| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ossera™ AFX Instrumentation | 6744-4060-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-5164-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-3868-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-5222-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-4460-N | FDA UDI | Class II | Active |
| restor3d Utility Wedge | 1105-2723120005R | FDA UDI | Class II | Active |
| restor3d Veritas rTSA Instrumentation | 5500-1103 | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-1015 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-5272-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-3448-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-3868-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-3864-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-3024-N | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 2834-2004 | FDA UDI | Class II | Active |
| restor3d Osteotomy Wedge | 1100-001-20140507 | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-0012 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-1052-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-3414-N | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 3832-1311 | FDA UDI | Class II | Active |
| restor3d Kinos Axiom Total Ankle System | 1831.1110 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-4174-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-5172-N | FDA UDI | Class II | Active |
| Kinos Axiom | 3801-1412 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-4146-N | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 3832-2410 | FDA UDI | Class II | Active |
| Kinos Axiom | 2831-3003 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-4038-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-3656-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-4666-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-5060-N | FDA UDI | Class II | Active |
| Kinos Axiom | 5801.0010 | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Cervical Cage Trial | 6110-16130807 | FDA UDI | Class I | Active |
| Ossera™ AFX Instrumentation | 6743-3444-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-3874-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-2016-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-4236-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-1050-N | FDA UDI | Class II | Active |
| restor3d Osteotomy Wedge | 1101-20180818 | FDA UDI | Class II | Active |
| restor3d Cervical Cage | 1110-001-14110507 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-3842-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-4258-N | FDA UDI | Class II | Active |
| restor3d Lumbar Implant | 1113-S1015 | FDA UDI | Class II | Active |
| restor3d Veritas rTSA Instrumentation | 6500-3038 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-3038-N | FDA UDI | Class II | Active |
| Kinos Instrumentation | 5801-7008 | FDA UDI | Class II | Active |
| restor3d Total Talus Replacement | 1102-03 | FDA UDI | Unclassified | Active |
| Ossera™ AFX | 1740-3814-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-3640-N | FDA UDI | Class II | Active |
| restor3d Utility Wedge | 1105-2719100505L | FDA UDI | Class II | Active |
| restor3d Cervical Cage | 1110-001-16130907 | FDA UDI | Class II | Active |
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