Reger Medizintechnik, GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Reger Medizintechnik, GmbH has 1 FDA 510(k) cleared medical devices. Based in Villingendorf, DE.
Last cleared in 2023. Active since 2023. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Reger Medizintechnik, GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Reger Medizintechnik, GmbH
1 devices