Gelesis, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gelesis, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Plenity
2
Total
1
Cleared
1
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) Regulatory Record - Gelesis, Inc.
2 devices