Medical Device Manufacturer · LI , Triesen

Bemer Int AG - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2017

Total

Cleared

Denied

Bemer Int AG has 4 FDA 510(k) cleared medical devices. Based in Triesen, LI.

Last cleared in 2023. Active since 2017. Primary specialty: Physical Medicine.

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

FDA 510(k) cleared devices by Bemer Int AG

4 devices

1-4 of 4