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Sign in to claim this brandWenzel Spine
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 2535 Brockton Dr Ste 450, Austin, TX, 78758
- Website
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- —
- —
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3006172536
- DUNS Number
- —
Catalogue (135)
Page 3 of 3| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| primaLOK FF | 800-1210 | FDA UDI | Class I | Active |
| VariLift-LX | CIE3-A128 | FDA UDI | Class II | Active |
| VariLift-LX | CIE3-11-28-00 | FDA UDI | Class II | Active |
| VariLift-LX | CIE3-14-24-00 | FDA UDI | Class II | Active |
| primaLOK-SP | 800-0312 | FDA UDI | Class I | Active |
| primaLOK SP | 800-0106-00 | FDA UDI | Class II | Active |
| primaLOK FF | 800-1206 | FDA UDI | Class I | Active |
| VariLift-C | CIC1-A744 | FDA UDI | Class I | Active |
| VariLift-L | CIE2-11-24-00 | FDA UDI | Class II | Active |
| primaLOK SP | 800-0828-00 | FDA UDI | Class II | Active |
| VariLift-C | CIC2-A744 | FDA UDI | Class I | Active |
| primaLOK-FF | 800-1201 | FDA UDI | Class I | Active |
| VariLift-L | CIE2-A423 | FDA UDI | Class I | Active |
| primaLOK-SP | 800-0315 | FDA UDI | Class I | Active |
| primaLOK SP | 800-0227 | FDA UDI | Class II | Active |
| primaLOK FF | 800-1211 | FDA UDI | U | Active |
| VariLift-L | CIE2-A023-C01 | FDA UDI | Class II | Active |
| VariLift-LX | CIE2-A012-C01 | FDA UDI | Class II | Active |
| VariLift-C | CIC1-7.5-12-00 | FDA UDI | Class II | Active |
| primaLOK SP | 800-0500 | FDA UDI | Class II | Active |
| VariLift-LX | CIE2-A017 | FDA UDI | Class II | Active |
| VariLift-C | CIC1-9.0-12-00 | FDA UDI | Class II | Active |
| VariLift-L | CIE2-13-24-00 | FDA UDI | Class II | Active |
| primaLOK FF | 800-1205 | FDA UDI | Class I | Active |
| primaLOK FF | 800-1202 | FDA UDI | Class I | Active |
| primaLOK FF | 800-1213 | FDA UDI | U | Active |
| VariLift-LX Interbody Fusion System, VariLift-C Interbody Fusion System | K180822 | FDA 510(k) | Class II | Active |
| VariLift®-C Interbody Fusion System | K231076 | FDA 510(k) | Class II | Active |
| primaLOK™ SP Interspinous Fusion System | K231807 | FDA 510(k) | Class II | Active |
| Varilift Cervical Interbody Fusion System | K111123 | FDA 510(k) | Class II | Active |
| Wenzel Spine Varilift Interbody Fusion System | K100820 | FDA 510(k) | Class II | Active |
| VariLift-L Interbody Fusion Device | K151900 | FDA 510(k) | Class II | Active |
| Varilift-L Interbody Fusion Device | K131296 | FDA 510(k) | Class II | Active |
| panaSIa SI Fusion System | K250247 | FDA 510(k) | Class II | Active |
| Varilift -c | K120603 | FDA 510(k) | Class II | Active |
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