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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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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
- 3011301313
- DUNS Number
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Catalogue (1774)
Page 35 of 36| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Focus | L-01-050 | FDA UDI | Class II | Active |
| Focus | PD-1000T-110 | FDA UDI | Class I | Active |
| Healix | SH-30-22 | FDA UDI | Class II | Active |
| Vertex | STK-1000T-008 | FDA UDI | Class I | Active |
| tangis | ACP-425-18F | FDA UDI | Class II | Active |
| nvt | TL-1135T-007 | FDA UDI | Class I | Active |
| nva | ALE-0610-S | FDA UDI | Class II | Active |
| Focus | PDR-550-025 | FDA UDI | Class II | Unknown |
| Focus | PDCR-850-095 | FDA UDI | Class II | Active |
| Healix | SH-25-24 | FDA UDI | Class II | Active |
| nva | AL-2534T-0618 | FDA UDI | Class I | Active |
| Retropsoas Electrode | ELEC2280 | FDA UDI | Class I | Active |
| PLIF - Posterior Lumbar Interbody Fusion Sysytem | PL-609-M | FDA UDI | Class II | Active |
| ACIF - Anterior Cervical Interbody Fusion System | AC-611-L | FDA UDI | Class II | Active |
| Anterior Lumbar Interbody Fusion System | AL-1216-L | FDA UDI | Class II | Active |
| PLIF - Posterior Lumbar Interbody Fusion Sysytem | PL-015-M | FDA UDI | Class II | Active |
| Retropsoas Electrode | ELEC1000-08 | FDA UDI | Class II | Active |
| Anterior Lumbar Interbody Fusion System | AL-0616-L | FDA UDI | Class II | Active |
| Earp Instruments | EARP-DS-001-12 | FDA UDI | Class I | Active |
| PLIF - Posterior Lumbar Interbody Fusion Sysytem | PL-611-L | FDA UDI | Class II | Active |
| Anterior Lumbar Interbody Fusion System | AL-1220-S | FDA UDI | Class II | Active |
| ACIF - Anterior Cervical Interbody Fusion System | AC-605-L | FDA UDI | Class II | Active |
| Earp Instruments | EARP-IC_2240 | FDA UDI | Class I | Active |
| PLIF - Posterior Lumbar Interbody Fusion Sysytem | PL-012-L | FDA UDI | Class II | Active |
| ACIF - Anterior Cervical Interbody Fusion System | AC-610-S | FDA UDI | Class II | Active |
| PLIF - Posterior Lumbar Interbody Fusion Sysytem | PL-014-S | FDA UDI | Class II | Active |
| Watershed Idea Foundry | Watershed-01 | FDA UDI | Class I | Active |
| ACIF - Anterior Cervical Interbody Fusion System | AC-012-S | FDA UDI | Class II | Active |
| Earp Instruments | EARP-DS-001-08 | FDA UDI | Class I | Active |
| ACIF - Anterior Cervical Interbody Fusion System | AC-008-L | FDA UDI | Class II | Active |
| Earp Instruments | EARP-DC | FDA UDI | Class I | Active |
| PLIF - Posterior Lumbar Interbody Fusion Sysytem | PL-007-M | FDA UDI | Class II | Active |
| EARP Retractor | EARP-R_001-120 | FDA UDI | Class I | Active |
| PLIF - Posterior Lumbar Interbody Fusion Sysytem | PL-009-M | FDA UDI | Class II | Active |
| TLIF - Transforaminal Lumbar Interbody Fusion System | TL-712-T | FDA UDI | Class II | Active |
| Earp Instruments | EARP-IC_1435 | FDA UDI | Class I | Active |
| Trigon PEEK HA Wedges | K243231 | FDA 510(k) | Class II | Active |
| Caliber Intramedullary Fixation System | K242896 | FDA 510(k) | Class II | Active |
| enHAnce PEEK Bunion System | K253718 | FDA 510(k) | Class II | Active |
| SnapHammer Hammertoe Correction System | K250613 | FDA 510(k) | Class II | Active |
| Trigon HA Wedge Fixation System | K220197 | FDA 510(k) | Class II | Active |
| Vortex5 Tailor's Bunion Correction System | K260291 | FDA 510(k) | Class II | Active |
| EARP Nerve Cuff Electrode | K230853 | FDA 510(k) | Class II | Active |
| nvc | K190380 | FDA 510(k) | Class II | Active |
| Trigon Trigon HA Stand-Alone Wedge Fixation System | K234116 | FDA 510(k) | Class II | Active |
| Integral Titanium Cervical Interbody | K222015 | FDA 510(k) | Class II | Active |
| FOCUS Pedicle Screw System | K180458 | FDA 510(k) | Class II | Active |
| nvc | K142328 | FDA 510(k) | Class II | Active |
| Javelin Tailor's Bunion Fixation System | K202657 | FDA 510(k) | Class II | Active |
| Vector Hammertoe Correction System | K201850 | FDA 510(k) | Class II | Active |
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