Medical Device Manufacturer · DE , Tuttingen

Evonos GmbH & Co. KG - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2024
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.

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