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Sign in to claim this brandVY SPINE LLC
US
Last updated May 24, 2026
What VY SPINE LLC makes
Vy Spine LLC manufactures spinal fixation devices, including non-sterile bone-screw systems for internal spinal stabilization, non-bioabsorbable spinal plates, and polymeric interbody fusion cages for intervertebral support. Their portfolio also includes spinal screws, reusable internal fixation procedure kits, spinal implant trials, and connectors and rods for spinal fixation systems. Examples include the Reliance Lumbar IBF System, VySpan™, and ClariVy™, designed for lumbar and cervical spine applications.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s UdL (UDI) database. The company operates within the United States, adhering to applicable U.S. medical device compliance standards.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- reliance-medical.net
- —
- —
- [email protected]
- Phone
- 801-295-3280
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 049592888
Catalogue (765)
Page 16 of 16| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| ClariVy™ Cervical IBF System | K231836 | FDA 510(k) | Class II | Active |
| VySpan™ PCT System | K232167 | FDA 510(k) | Class II | Active |
| LumiVy™ Lumbar IBF System | K233807 | FDA 510(k) | Class II | Active |
| Vy Spine ClariVy Cervical IBF System | K212715 | FDA 510(k) | Class II | Active |
| UniVy OsteoVy Cervical IBF System | K221162 | FDA 510(k) | Class II | Active |
| VySpan™ PCT System | K223852 | FDA 510(k) | Class II | Active |
| VyLink™ Spinal Screw System | K231744 | FDA 510(k) | Class II | Active |
| LumiVy Lumbar IBF System | K212930 | FDA 510(k) | Class II | Active |
| UniVy™ OsteoVy™-Ti Cervical IBF System | K223513 | FDA 510(k) | Class II | Active |
| DiversiVy™ Facet Screw System | K253432 | FDA 510(k) | U | Active |
| VyLink™ Spinal Screw System | K213750 | FDA 510(k) | Class II | Active |
| VyPlate Anterior Cervical Plate System | K221572 | FDA 510(k) | Class II | Active |
| FortiVy™ OsteoVy™ Lumbar IBF | K241783 | FDA 510(k) | Class II | Active |
| VyBrate™ VBR System | K253158 | FDA 510(k) | Class II | Active |
| Vy Spine™ VyLam™ Laminoplasty System | K232471 | FDA 510(k) | Class II | Active |
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