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Sign in to claim this brandSpine Vision, Inc.
US
Last updated May 23, 2026
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Catalogue (2379)
Page 48 of 48| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| C3® Acps | C1-A217/3N1 | FDA UDI | Class I | Active |
| C3® Acps | C1-C4016 | FDA UDI | Class II | Active |
| C3® Acps | C1-P3 0720 | FDA UDI | Class II | Active |
| P Cage - T Cage | P CAGE H16-L25-A00 | FDA UDI | Class II | Active |
| C3® Acps | C1-P1 0365 | FDA UDI | Class II | Active |
| P Cage - T Cage | P CAGE H10-L21-A00 | FDA UDI | Class II | Active |
| C3® Acps | C1-D4016 | FDA UDI | Class II | Active |
| P Cage - T Cage | TL1-U13 | FDA UDI | Class II | Active |
| C3® Acps | C1-L4 0890 | FDA UDI | Class II | Active |
| P Cage - T Cage | P CAGE H07-L21-A04 | FDA UDI | Class II | Active |
| U.l.i.s™ | IS1-A317 | FDA UDI | Class II | Active |
| C3® Acps | C1-L4 1050 | FDA UDI | Class II | Active |
| C3® Acps | C1-C4014 | FDA UDI | Class II | Active |
| C3® Acps | C1-P4 1010 | FDA UDI | Class II | Active |
| U.l.i.s™ | SD-RACK1 | FDA UDI | Class I | Active |
| U.l.i.s™ | IS1-ID | FDA UDI | Class II | Active |
| P Cage - T Cage | P CAGE H12-L25-A04 | FDA UDI | Class II | Active |
| Uni-T Uni-Thread Spinal System | K021510 | FDA 510(k) | Class II | Active |
| Plus Pivot Link Universal System | K021507 | FDA 510(k) | Class II | Active |
| P.l.u.s. System (pivot Link Universal System) | K013312 | FDA 510(k) | Class II | Active |
| Plus Pivot Link Universal System | K022271 | FDA 510(k) | Class II | Active |
| Spacevision Cage System | K042930 | FDA 510(k) | Class II | Active |
| Plus Pivot Link Universal System | K032398 | FDA 510(k) | Class II | Active |
| Uni-Thread Spinal System | K042640 | FDA 510(k) | Class II | Active |
| Plus Pivot Link Universal System | K033508 | FDA 510(k) | Class II | Active |
| C3 Anterior Cervical Plate System | K012881 | FDA 510(k) | Class II | Active |
| Uni-T Spinal System | K013301 | FDA 510(k) | Class II | Active |
| Uni-Thread Spinal System | K052406 | FDA 510(k) | Class II | Active |
| Pediguard Nerve Detector System | K030526 | FDA 510(k) | Class II | Active |
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