Medical Device Manufacturer · US , Boston , MA

Gelesis, Inc. - FDA 510(k) Cleared Devices

2 submissions · 1 cleared · Since 2019

Total

Cleared

Denied

Gelesis, Inc. has 1 FDA 510(k) cleared medical devices. Based in Boston, US.

Latest FDA clearance: Jan 2024. Active since 2019. Primary specialty: Gastroenterology & Urology.

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

FDA 510(k) cleared devices by Gelesis, Inc.

2 devices

1-2 of 2