Dio Corporation - FDA 510(k) Cleared Devices

Dio Corporation has 14 FDA 510(k) cleared dental devices. Based in Los Angeles, US.

Last cleared in 2023. Active since 2010.

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

Regulatory submissions have been managed by Dio USA, Withus Group, Inc. and Provision Consulting Group, Inc..