COMPANY
Augmedics
Augmedics is listed on ClinicalTrials.gov as the lead sponsor of 1 study; the most recently updated is “Pedicle Screw Placement With XVS” (no phase, completed), in Spine Fusion. From public records Source · Oct 12, 2026
Timeline
- FDA FDA 510(k) clearance: xvision Spine system — K261854, Jul 31, 2026. Applicant at approval: Augmedics, Ltd. source ↗
- FDA FDA 510(k) clearance: xvision Spine system — K251639, Oct 3, 2025. Applicant at approval: Augmedics, Ltd. source ↗
- FDA FDA 510(k) clearance: xvision Spine system — K250255, Mar 13, 2025. Applicant at approval: Augmedics, Ltd. source ↗
- FDA FDA 510(k) clearance: xvision Spine System — K241481, Oct 16, 2024. Applicant at approval: Augmedics, Ltd. source ↗
FDA records (last 2 years)
- FDA 510(k) clearance: xvision Spine system — K261854, Jul 31, 2026. Applicant at approval: Augmedics, Ltd. source ↗
- FDA 510(k) clearance: xvision Spine system — K251639, Oct 3, 2025. Applicant at approval: Augmedics, Ltd. source ↗
- FDA 510(k) clearance: xvision Spine system — K250255, Mar 13, 2025. Applicant at approval: Augmedics, Ltd. source ↗
- FDA 510(k) clearance: xvision Spine System — K241481, Oct 16, 2024. Applicant at approval: Augmedics, Ltd. source ↗
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