Pro3Dure Medical is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Pro3Dure Medical - FDA 510(k) Cleared Devices
Recent clearances: GR Resin System MSI
1
Total
1
Cleared
0
Denied
Pro3Dure Medical has 1 FDA 510(k) cleared medical devices. Based in Iserlohn, DE.
Latest FDA clearance: Aug 2024. Active since 2024. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Pro3Dure Medical Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Kontoudis Regulatory Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Pro3Dure Medical
1 devices