Dentalhitec is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Dentalhitec - FDA 510(k) Cleared Devices
Recent clearances: QuickSleeper 5
1
Total
1
Cleared
0
Denied
Dentalhitec has 1 FDA 510(k) cleared medical devices. Based in Mazieres En Mauges, FR.
Latest FDA clearance: Aug 2025. Active since 2025. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Dentalhitec Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Qrs Solutions, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Dentalhitec
1 devices