Medical Device Manufacturer · US , Winona , MN

Comfortex, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1985

Total

Cleared

Denied

Comfortex, Inc. has 4 FDA 510(k) cleared medical devices. Based in Winona, US.

Historical record: 4 cleared submissions from 1985 to 1986. Primary specialty: Neurology.

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

FDA 510(k) Regulatory Record - Comfortex, Inc.

4 devices

1-4 of 4