Medical Device Manufacturer · US , Houston , TX

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

4 submissions · 4 cleared · Since 1987

Total

Cleared

Denied

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

Historical record: 4 cleared submissions from 1987 to 1990. Primary specialty: Dental.

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

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

4 devices

1-4 of 4