Medovent GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Medovent GmbH - FDA 510(k) Cleared Devices
Recent clearances: Reaxon Plus
2
Total
2
Cleared
0
Denied
Medovent GmbH has 2 FDA 510(k) cleared medical devices. Based in Mainz, DE.
Historical record: 2 cleared submissions from 2015 to 2018. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Medovent GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medovent GmbH
2 devices