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.
510(k) submissions have been managed by QSR Consulting as regulatory consultant.
1 devices