Brius Technologies, Inc. - FDA 510(k) Cleared Devices

Brius Technologies, Inc. has 2 FDA 510(k) cleared medical devices. Based in Carrollton, US.

Last cleared in 2021. Active since 2021. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Brius Technologies, Inc. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Prime Path Medtech and Medavice, Inc..