Brius Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Brius Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: BRIUS Planner Software, BRIUS Clear Aligners
2
Total
2
Cleared
0
Denied
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 Medavice, Inc. and Prime Path Medtech.
FDA 510(k) Regulatory Record - Brius Technologies, Inc.
2 devices