COMPANY
Xenix Medical
Timeline
- FDA FDA 510(k) clearance: RIVA® Posterior Fixation System with NanoACTIV Surface Technology; RIVA® Anchor Sacroiliac Fixation System with NanoACTIV Surface Technology — K262193, Sep 14, 2026. Applicant at a source ↗
- FDA FDA 510(k) clearance: LUX Expandable Lumbar Interbody System — K253583, Feb 23, 2026. Applicant at approval: Xenix Medical. source ↗
FDA records (last 2 years)
- FDA 510(k) clearance: RIVA® Posterior Fixation System with NanoACTIV Surface Technology; RIVA® Anchor Sacroiliac Fixation System with NanoACTIV Surface Technology — K262193, Sep 14, 2026. Applicant at approval: Xenix Medical. source ↗
- FDA 510(k) clearance: LUX Expandable Lumbar Interbody System — K253583, Feb 23, 2026. Applicant at approval: Xenix Medical. source ↗