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.

Reshape Lifesciences is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Reshape Lifesciences

4 devices

1-4 of 4