Alber GmbH is one of 470 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Alber GmbH - FDA 510(k) Cleared Devices
Recent clearances: e-motion M25, e-Motion M25, SMOOV O10
5
Total
5
Cleared
0
Denied
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.
Regulatory submissions have been managed by Beo Medconsulting Berlin GmbH and Mdi Consultants, Inc..
FDA 510(k) Regulatory Record - Alber GmbH
5 devices