Medical Device Manufacturer · DE , Germany

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

1 submissions · 1 cleared · Since 1991

Total

Cleared

Denied

Ionos GmbH & Co. KG has 1 FDA 510(k) cleared medical devices. Based in Germany, DE.

Historical record: 1 cleared submissions from 1991 to 1991. Primary specialty: Ear, Nose, Throat.

Browse the FDA 510(k) cleared devices submitted by Ionos GmbH & Co. KG Filter by specialty or product code using the sidebar.

Ionos GmbH & Co. KG is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Ionos GmbH & Co. KG

1 devices

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