GI Windows Surgical is one of 26109 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
GI Windows Surgical - FDA 510(k) Cleared Devices
Recent clearances: GI Windows Flexagon Plus OTOLoc System
1
Total
1
Cleared
0
Denied
GI Windows Surgical has 1 FDA 510(k) cleared medical devices. Based in Canton, US.
Latest FDA clearance: Oct 2026. Active since 2026. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by GI Windows Surgical Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - GI Windows Surgical
1 devices