Medical Device Manufacturer · US , San Clemente , CA

Reshape Lifesciences - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2022

Total

Cleared

Denied

Reshape Lifesciences has 4 FDA 510(k) cleared medical devices. Based in San Clemente, US.

Latest FDA clearance: May 2024. Active since 2022. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Reshape Lifesciences Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Reshape Lifesciences

4 devices

1-4 of 4