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US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 149 W Michigan St, Orlando, FL, 32806
- Website
- —
- —
- —
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3012429289
- DUNS Number
- —
Catalogue (933)
Page 1 of 19| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Xenix Medical Sacroiliac Fixation System | SS1-A3-000030 | FDA UDI | Class II | Active |
| Ti3D CERVICAL | B221-08 | FDA UDI | Class II | Active |
| Ti3D CERVICAL | C1412-09 | FDA UDI | Class II | Active |
| NeoFuse HA Enhanced PLIF/TLIF | A2410-11 | FDA UDI | Class II | Unknown |
| neoWave C | 20-TFX-5209 | FDA UDI | Class I | Active |
| RIVA Posterior Fixation System | FG1-A3-000092 | FDA UDI | Class I | Active |
| SOLACE Sacroiliac Fixation System | SS1-A2-000720 | FDA UDI | Class II | Active |
| RIVA Posterior Fixation System | FG1-A3-000074 | FDA UDI | Class I | Active |
| SOLACE Sacroiliac Fixation System | SS1-A2-000361 | FDA UDI | Class II | Active |
| SOLACE Sacroiliac Fixation System | SS1-A2-000603 | FDA UDI | Class II | Active |
| neoWave C | 20-CFX-9412 | FDA UDI | Class II | Active |
| neoWave LS | 23-LCN-2506 | FDA UDI | Class II | Active |
| neoWave C | 20-TFX-5210 | FDA UDI | Class I | Active |
| neoWave LS | 23-LCT-2513 | FDA UDI | Class II | Active |
| neoWave C | 20-TFN-5211 | FDA UDI | Class I | Active |
| NeoFuse HA Enhanced PLIF/TLIF | A3010-07 | FDA UDI | Class II | Unknown |
| SOLACE Sacroiliac Fixation System | SS1-A2-000602 | FDA UDI | Class II | Active |
| neoWave C | 20-CFT-7305 | FDA UDI | Class II | Active |
| NeoFuse HA Enhanced PLIF/TLIF | A2410-12 | FDA UDI | Class II | Unknown |
| SOLACE Sacroiliac Fixation System | SS1-A2-000510 | FDA UDI | Class II | Active |
| NeoFuse HA Enhanced PLIF/TLIF | A2010-13 | FDA UDI | Class II | Unknown |
| NeoFuse Ti3D PLIF/TLIF | C2410-11 | FDA UDI | Class II | Unknown |
| neoWave C | 20-TFN-7308 | FDA UDI | Class I | Active |
| RIVA Posterior Fixation System | FG1-B0-001290 | FDA UDI | Class I | Active |
| RIVA Posterior Fixation System | FG1-32-055040 | FDA UDI | Class II | Active |
| Ti3D CERVICAL | B22-05 | FDA UDI | Class I | Active |
| NeoFuse HA Enhanced PLIF/TLIF | A2010-17 | FDA UDI | Class II | Unknown |
| neoWave C | 20-TFN-9406 | FDA UDI | Class I | Active |
| NeoFuse HA Enhanced PLIF/TLIF | A2410-08 | FDA UDI | Class II | Unknown |
| neoWave C | 20-CFT-3208 | FDA UDI | Class II | Active |
| neoWave LS | 23-K01-0213 | FDA UDI | Class I | Active |
| RIVA Posterior Fixation System | FG1-A3-100020 | FDA UDI | Class II | Active |
| Xenix Medical Sacroiliac Fixation System | SS1-A2-000411 | FDA UDI | Class II | Active |
| NeoFuse HA Enhanced PLIF/TLIF | A2410-18 | FDA UDI | Class II | Unknown |
| neoWave LS | 23-LTT-2513 | FDA UDI | Class II | Active |
| SOLACE Sacroiliac Fixation System | SS1-32-012105 | FDA UDI | Class II | Active |
| neoWave LS | 23-K01-0215 | FDA UDI | Class I | Active |
| neoWave LS | 23-LCX-2511 | FDA UDI | Class II | Active |
| neoWave LS | 23-K01-0309 | FDA UDI | Class I | Active |
| Ti3D CERVICAL | C1613-10 | FDA UDI | Class II | Active |
| SOLACE Sacroiliac Fixation System | SS1-A1-000042 | FDA UDI | Class II | Active |
| neoWave C | 20-TFN-9405 | FDA UDI | Class I | Active |
| neoWave LS | 23-K01-0211 | FDA UDI | Class I | Active |
| neoWave C | 20-CFT-5212 | FDA UDI | Class II | Active |
| neoWave LS | 23-LCX-2217 | FDA UDI | Class II | Active |
| neoWave C | 20-CFN-7311 | FDA UDI | Class II | Active |
| neoWave C | 20-CFN-7306 | FDA UDI | Class II | Active |
| neoWave C | 20-TFT-9405 | FDA UDI | Class I | Active |
| Ti3D CERVICAL | C1412-08 | FDA UDI | Class II | Active |
| NeoFuse Ti3D PLIF/TLIF | C3012-11 | FDA UDI | Class II | Unknown |
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