Medical Device Manufacturer · US , New Brighton , MN

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

2 submissions · 2 cleared · Since 2005

Total

Cleared

Denied

Compex Technologies, Inc. has 2 FDA 510(k) cleared medical devices. Based in New Brighton, US.

Historical record: 2 cleared submissions from 2005 to 2007. Primary specialty: Physical Medicine.

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

Compex Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

2 devices

1-2 of 2