Medical Device Manufacturer · US , Mission Viejo , CA

Polymed Therapeutics, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2012

Total

Cleared

Denied

Polymed Therapeutics, Inc. has 5 FDA 510(k) cleared medical devices. Based in Mission Viejo, US.

Historical record: 5 cleared submissions from 2012 to 2014. Primary specialty: Chemistry.

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

510(k) submissions have been managed by Lsi International as regulatory consultant.

Polymed Therapeutics, Inc. is one of 12957 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Polymed Therapeutics, Inc.

5 devices

1-5 of 5

Data Source

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

Last updated: Sep 16, 2026