Medical Device Manufacturer · US , Centereach , NY

Protech Professional Products, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1993

Recent clearances: ProTech Plus, PERMAFLEX PERMANENT SOFT DENTURE RELINER

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Protech Professional Products, Inc. Dental ✕

2 devices

1-2 of 2

Cleared Oct 21, 2015

Cleared Mar 31, 1993

PERMAFLEX PERMANENT SOFT DENTURE RELINER

Data Source

Sourced from the FDA 510(k) public files . 176,583 total devices indexed.

Last updated: Sep 22, 2026