Medical Device Manufacturer · BE , Nivelles

G-Flex Europe Sprl - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2022

Total

Cleared

Denied

G-Flex Europe Sprl has 2 FDA 510(k) cleared medical devices. Based in Nivelles, BE.

Last cleared in 2023. Active since 2022. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by G-Flex Europe Sprl Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by G-Flex Europe Sprl

2 devices

1-2 of 2