Medical Device Manufacturer · US , Duarte , CA

Temrex Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1985

Total

Cleared

Denied

Temrex Corp. has 2 FDA 510(k) cleared medical devices. Based in Duarte, US.

Historical record: 2 cleared submissions from 1985 to 2012. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Temrex Corp. Filter by specialty or product code using the sidebar.

Temrex Corp. 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 - Temrex Corp.

2 devices

1-2 of 2