Medical Device Manufacturer · CH , Bern

Cascination AG - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2015

Total

Cleared

Denied

Cascination AG has 7 FDA 510(k) cleared medical devices. Based in Bern, CH.

Latest FDA clearance: Sep 2026. Active since 2015. Primary specialty: Ear, Nose, Throat.

Browse the FDA 510(k) cleared devices submitted by Cascination AG Filter by specialty or product code using the sidebar.

Cascination AG is one of 130 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Cascination AG

7 devices

1-7 of 7