Mevis Medical Solutions AG is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mevis Medical Solutions AG - FDA 510(k) Cleared Devices
Recent clearances: MeVis Liver Suite, Veolity
6
Total
6
Cleared
0
Denied
Mevis Medical Solutions AG has 6 FDA 510(k) cleared medical devices. Based in Pewaukee, US.
Last cleared in 2023. Active since 2011. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Mevis Medical Solutions AG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mevis Medical Solutions AG
6 devices