Medical Device Manufacturer · US , Glenview , IL

Precident Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1991

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Precident Corp. Dental ✕

2 devices

1-2 of 2

Cleared Oct 02, 1991

PDI PARALLEL SIDED POST KIT

Cleared Sep 30, 1991

Data Source

Sourced from the FDA 510(k) public files . 175,972 total devices indexed.

Last updated: Apr 28, 2026