Kaltenbach & Voigt GmbH - FDA 510(k) Cleared Devices

Kaltenbach & Voigt GmbH has 9 FDA 510(k) cleared medical devices. Based in Orange, US.

Historical record: 9 cleared submissions from 2011 to 2019. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Kaltenbach & Voigt GmbH Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Kavo Dental Technologies, LLC as regulatory consultant.