Dentona AG - FDA 510(k) Cleared Devices

Dentona AG has 1 FDA 510(k) cleared medical devices. Based in Dortmund, DE.

Last cleared in 2023. Active since 2023. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Dentona AG Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Apf Consulting as regulatory consultant.