Evonos GmbH & Co. KG is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Evonos GmbH & Co. KG - FDA 510(k) Cleared Devices
Recent clearances: evoDrill Cranial Perforator
1
Total
1
Cleared
0
Denied
Evonos GmbH & Co. KG has 1 FDA 510(k) cleared medical devices. Based in Tuttingen, DE.
Latest FDA clearance: Mar 2024. Active since 2024. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Evonos GmbH & Co. KG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Evonos GmbH & Co. KG
1 devices