Medical Device Manufacturer · DE , Iserlohn

Pro3Dure Medical - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2024
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
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