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Sign in to claim this brandNVISION BIOMEDICAL TECHNOLOGIES, INC
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 12449 Silicon Dr, San Antonio, TX, 78249
- Website
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- —
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3011301313
- DUNS Number
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Catalogue (1774)
Page 36 of 36| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Quantum Anterior Cervical Plate | K210424 | FDA 510(k) | Class II | Active |
| Vector Hammertoe Correction System | K183055 | FDA 510(k) | Class II | Active |
| Healix Compression Screw System | K200914 | FDA 510(k) | Class II | Active |
| Trigon™ Ti Stand-Alone Wedge Fixation System | K192645 | FDA 510(k) | Class II | Active |
| Impact PEEK Union Nail System | K250646 | FDA 510(k) | Class II | Active |
| nva, nvp, nvt | K142594 | FDA 510(k) | Class II | Active |
| The Radian MIS Bunion System | K211650 | FDA 510(k) | Class II | Active |
| Trigon HA Stand-Alone Wedge Fixation System | K203445 | FDA 510(k) | Class II | Active |
| Vector® Hammertoe Correction System | K213421 | FDA 510(k) | Class II | Active |
| nva, nvp, and nvt | K193645 | FDA 510(k) | Class II | Active |
| nvc | K170074 | FDA 510(k) | Class II | Active |
| Impact PEEK Union Nail System | K252657 | FDA 510(k) | Class II | Active |
| Boundary Anterior Lumbar Buttress Plate | K173091 | FDA 510(k) | Class II | Active |
| Multi-Drive Interference Screw System | K200428 | FDA 510(k) | Class II | Active |
| SnapHammer Hammertoe Correction System | K231453 | FDA 510(k) | Class II | Active |
| EARP Interbody System | K212477 | FDA 510(k) | Class II | Active |
| nva, nvp, and nvt | K162426 | FDA 510(k) | Class II | Active |
| Tangis Anterior Cervical Plate | K161524 | FDA 510(k) | Class II | Active |
| Healix™ Compression Screw System | K182949 | FDA 510(k) | Class II | Active |
| Trigon HA Stand-Alone Wedge Fixation System | K193414 | FDA 510(k) | Class II | Active |
| Trigon™ HA Stand-Alone Wedge Fixation System | K223226 | FDA 510(k) | Class II | Active |
| 3D Printed PEEK Interbody System | K240250 | FDA 510(k) | Class II | Active |
| VERTEX Nitinol Staple System | K182943 | FDA 510(k) | Class II | Active |
| ToeJack MIS Bunion System | K253423 | FDA 510(k) | Class II | Active |
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