Medical Device Manufacturer · US , Westwood , MA

GI Windows, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2025

Total

Cleared

Denied

GI Windows, Inc. has 4 FDA 510(k) cleared medical devices. Based in Westwood, US.

Latest FDA clearance: Jan 2026. Active since 2025. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by GI Windows, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by GI Windows, Inc.

4 devices

1-4 of 4