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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
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- EUDAMED SRN
- —
- FDA FEI Number
- 3014833750
- DUNS Number
- —
Catalogue (2760)
Page 28 of 56| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| restor3d Cervical Cage | 1110-16130707 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-4456-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-4072-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-4046-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-4656-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-4246-N | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 3832-1415 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-3444-N | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-0050 | FDA UDI | Class II | Active |
| restor3d Utility Wedge | 1105-2723121005L | FDA UDI | Class II | Active |
| Veritas rTSA | 3500-136U1 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-4642-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-3152-N | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Cervical Cage Trial | 6110-17151207 | FDA UDI | Class I | Active |
| restor3d Osteotomy Wedge | 1100-002-22140607 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-4448-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-2068-N | FDA UDI | Class II | Active |
| restor3d Kinos Axiom PSR | 5831-9001 | FDA UDI | Class II | Active |
| restor3d Osteotomy Wedge | 1100-002-22140715 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-3662-N | FDA UDI | Class II | Active |
| restor3d Veritas rTSA Instrumentation | 5500-3111 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-3840-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-4036-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-4662-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-3452-N | FDA UDI | Class II | Active |
| Veritas rTSA | 1505-4858 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-3642-N | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Cervical Cage Trial | 6110-14111207 | FDA UDI | Class I | Active |
| Kinos Instrumentation | 5871-2720 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-3420-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-4042-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-2022-N | FDA UDI | Class II | Active |
| restor3d Utility Wedge | 1105-2719121005R | FDA UDI | Class II | Active |
| Kinos Instrumentation | 5801-2122 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-3144-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-4016-N | FDA UDI | Class II | Active |
| restor3d Veritas rTSA Instrumentation | 5500-2301 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-4652-N | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-1017 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-2014-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-4222-N | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-0051 | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 3832-1206 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-2032-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-4060-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-4018-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-3852-N | FDA UDI | Class II | Active |
| restor3d, Disposable Instrument, Cervical Cage Trial | 6110-001-14111007 | FDA UDI | Class I | Active |
| Kinos Axiom Total Ankle Replacement | 1834-0020 | FDA UDI | Class II | Active |
| restor3d Lumbar Implant | 1113-S1418 | FDA UDI | Class II | Active |
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