Medical Device Manufacturer · US , Port Townsend , WA

Fem Suite, LLC - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2007

Total

Cleared

Denied

Fem Suite, LLC has 2 FDA 510(k) cleared medical devices. Based in Port Townsend, US.

Historical record: 2 cleared submissions from 2007 to 2010. Primary specialty: Obstetrics & Gynecology.

Browse the FDA 510(k) cleared devices submitted by Fem Suite, LLC Filter by specialty or product code using the sidebar.

Fem Suite, LLC 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 - Fem Suite, LLC

2 devices

1-2 of 2

Data Source

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

Last updated: Apr 28, 2026