Ivoclar Vivadent, AG - FDA 510(k) Cleared Devices

Ivoclar Vivadent, AG has 31 FDA 510(k) cleared dental devices. Based in Amherst, US.

Last cleared in 2022. Active since 2004.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Ivoclar Vivadent, Inc. as regulatory consultant.