Reger Medizintechnik, GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Reger Medizintechnik, GmbH - FDA 510(k) Cleared Devices
Recent clearances: REGER Nebulizer Irrigation Cannula
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.
FDA 510(k) Regulatory Record - Reger Medizintechnik, GmbH
1 devices