Mediaire GmbH is one of 385 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Mediaire GmbH - FDA 510(k) Cleared Devices
Recent clearances: mdprostate
1
Total
1
Cleared
0
Denied
Mediaire GmbH has 1 FDA 510(k) cleared medical devices. Based in Berlin, DE.
Latest FDA clearance: Aug 2026. Active since 2026. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Mediaire GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mediaire GmbH
1 devices