Medical Device Manufacturer · US , Glenview , IL

American Pro Latex, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1990

Total

Cleared

Denied

American Pro Latex, Inc. has 5 FDA 510(k) cleared medical devices. Based in Glenview, US.

Historical record: 5 cleared submissions from 1990 to 1997. Primary specialty: General Hospital.

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

American Pro Latex, Inc. 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 - American Pro Latex, Inc.

5 devices

1-5 of 5

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: Apr 27, 2026