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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 18 of 56| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ossera™ AFX Instrumentation | 6744-5044-N | FDA UDI | Class II | Active |
| restor3d Disposable Trial Kit | 4101-010-0101 | FDA UDI | Class I | Active |
| Kinos Axiom Instrumentation | 5801-0902 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-4274-N | FDA UDI | Class II | Active |
| Kinos Instrumentation | 5871-2723 | FDA UDI | Class II | Active |
| restor3d Veritas rTSA Instrumentation | 5500-H32U3 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-3614-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-4458-N | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 2834-1002 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-4058-N | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-9208 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-3464-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-3866-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-3014-N | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-1014 | FDA UDI | Class II | Unknown |
| restor3d Lumbar Instrumentation | 5113-B3003 | FDA UDI | Class II | Active |
| Kinos Axiom Instrumentation | 5801-8106 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-4070-N | FDA UDI | Class II | Active |
| Kinos Axiom Total Ankle Replacement | 1834-0150 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-3836-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-4140-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6740-3442-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-3128-N | FDA UDI | Class II | Active |
| Kinos Aeros Total Ankle Replacement | 1832-0052 | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 3832-1408 | FDA UDI | Class II | Active |
| restor3d Osteotomy Wedge | 1101-009-20181218 | FDA UDI | Class II | Active |
| Kinos Axiom Total Ankle Replacement | 1834-0130 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-4058-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-4248-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-4048-N | FDA UDI | Class II | Active |
| Veritas rTSA | 1504-4818 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-3868-N | FDA UDI | Class II | Active |
| Kinos Total Ankle Replacement | 3832-1212 | FDA UDI | Class II | Active |
| restor3d Disposable Instrument, Wedge Trial | 6100-N02-A0910 | FDA UDI | Class I | Active |
| Kinos Axiom | 2831.0112 | FDA UDI | Class II | Unknown |
| Ossera™ AFX | 1740-4638-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1742-3648-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-5258-N | FDA UDI | Class II | Active |
| restor3d Lumbar Instrumentation | 5113-B1021 | FDA UDI | Class II | Active |
| Ossera™ AFX | 1743-4052-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1744-5274-N | FDA UDI | Class II | Active |
| restor3d Disposable Instrument | 6200-20 | FDA UDI | Class I | Active |
| Veritas rTSA | 1504-4858 | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-4046-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-5070-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6742-4664-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 6741-2801-N | FDA UDI | Class II | Active |
| Ossera™ AFX | 1740-4456-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6744-4114-N | FDA UDI | Class II | Active |
| Ossera™ AFX Instrumentation | 6743-3454-N | FDA UDI | Class II | Active |
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