Otto Bock Healthcare Products GmbH is one of 30 FDA 510(k) medical device manufacturers from Austria in the dataset, ranked by real submission volume.
Otto Bock Healthcare Products GmbH - FDA 510(k) Cleared Devices
Recent clearances: myosmart. (13E522), Myo Plus
3
Total
3
Cleared
0
Denied
Otto Bock Healthcare Products GmbH has 3 FDA 510(k) cleared medical devices. Based in Vienna, AT.
Latest FDA clearance: Apr 2026. Active since 2015. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Otto Bock Healthcare Products GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Otto Bock Healthcare Products GmbH
3 devices