Medical Device Manufacturer · US , Mchenry , IL

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

6 submissions · 6 cleared · Since 1979

Total

Cleared

Denied

Briox Technologies, Inc. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 6 cleared submissions from 1979 to 1982. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) Regulatory Record - Briox Technologies, Inc.

6 devices

1-6 of 6