Virtual Incision is one of 13998 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Virtual Incision - FDA 510(k) Cleared Devices
Recent clearances: MIRA Surgical System
2
Total
1
Cleared
1
Denied
Virtual Incision has 1 FDA 510(k) cleared medical devices. Based in Lincoln, US.
Latest FDA clearance: Aug 2026. Active since 2024. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Virtual Incision Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Virtual Incision
2 devices