I3 Membrane GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
I3 Membrane GmbH - FDA 510(k) Cleared Devices
Recent clearances: i3 ONE (203100-S)
1
Total
1
Cleared
0
Denied
I3 Membrane GmbH has 1 FDA 510(k) cleared medical devices. Based in Radeberg, DE.
Last cleared in 2023. Active since 2023. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by I3 Membrane GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - I3 Membrane GmbH
1 devices