Simex Medizintechnik GmbH is one of 204 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Simex Medizintechnik GmbH - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Simex Medizintechnik GmbH has 3 FDA 510(k) cleared medical devices. Based in Deisslingen, DE.
Historical record: 3 cleared submissions from 2012 to 2016. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Simex Medizintechnik GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Simex Medizintechnik GmbH
3 devices