Tontarra Medizintechnik GmbH is one of 470 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Tontarra Medizintechnik GmbH - FDA 510(k) Cleared Devices
Recent clearances: Tontarra Punches and Rongeurs
1
Total
1
Cleared
0
Denied
Tontarra Medizintechnik GmbH has 1 FDA 510(k) cleared medical devices. Based in Wurmlingen, DE.
Latest FDA clearance: Sep 2026. Active since 2026. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Tontarra Medizintechnik GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tontarra Medizintechnik GmbH
1 devices