Alber GmbH - FDA 510(k) Cleared Devices

Alber GmbH has 5 FDA 510(k) cleared medical devices. Based in Albstadt, DE.

Last cleared in 2022. Active since 2016. Primary specialty: Physical Medicine.

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

510(k) submissions have been managed by Beo Medconsulting Berlin GmbH as regulatory consultant.