Medical Device Manufacturer · US , Beaverton , OR

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

5 submissions · 5 cleared · Since 1991

Total

Cleared

Denied

Simpex, Inc. has 5 FDA 510(k) cleared medical devices. Based in Beaverton, US.

Historical record: 5 cleared submissions from 1991 to 1992. Primary specialty: General Hospital.

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

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

5 devices

1-5 of 5