Gelesis SRL is one of 205 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Gelesis SRL - FDA 510(k) Cleared Devices
Recent clearances: Plenity-V (MC0979 / GS110)
1
Total
1
Cleared
0
Denied
Gelesis SRL has 1 FDA 510(k) cleared medical devices. Based in Calimera, IT.
Latest FDA clearance: Oct 2026. Active since 2026. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Gelesis SRL Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Gelesis SRL
1 devices