Pro3dure Medical GmbH is one of 516 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Pro3dure Medical GmbH - FDA 510(k) Cleared Devices
Recent clearances: THERMEO® I MSI, Thermeo System, GR Splint Resin System
5
Total
5
Cleared
0
Denied
Pro3dure Medical GmbH has 5 FDA 510(k) cleared medical devices. Based in Iserlohn, DE.
Latest FDA clearance: Sep 2026. Active since 2020. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Pro3dure Medical GmbH Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Regulatory and Quality Solutions, LLC and Kontoudis Consulting, LLC.
FDA 510(k) Regulatory Record - Pro3dure Medical GmbH
5 devices