Miha Bodytec GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Miha Bodytec GmbH - FDA 510(k) Cleared Devices
Recent clearances: Miha Bodytec II, miha bodytec II, Miha Bodytec II
3
Total
3
Cleared
0
Denied
Miha Bodytec GmbH has 3 FDA 510(k) cleared medical devices. Based in Gersthofen, DE.
Last cleared in 2022. Active since 2019. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Miha Bodytec GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Iuvo Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Miha Bodytec GmbH
3 devices