COMPANY
FDA-cleared device company
Location: Austin, TX · source · Oct 15, 2026
Profile checked Oct 10, 2026
Timeline
- FDA FDA 510(k) clearance: VariLift-C Cervical Interbody Fusion System — K262595, Aug 26, 2026. Applicant at approval: Wenzel Spine, Inc. source ↗
- FDA FDA 510(k) clearance: panaSIa SI Fusion System — K250247, Jul 9, 2025. Applicant at approval: Wenzel Spine, Inc. source ↗
FDA records (last 2 years)
- FDA 510(k) clearance: VariLift-C Cervical Interbody Fusion System — K262595, Aug 26, 2026. Applicant at approval: Wenzel Spine, Inc. source ↗
- FDA 510(k) clearance: panaSIa SI Fusion System — K250247, Jul 9, 2025. Applicant at approval: Wenzel Spine, Inc. source ↗
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