Medical Device Manufacturer · US , Neenah , WI

Tidi Products,Llc - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2010

Total

Cleared

Denied

Tidi Products,Llc has 3 FDA 510(k) cleared medical devices. Based in Neenah, US.

Historical record: 3 cleared submissions from 2010 to 2014. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Tidi Products,Llc Filter by specialty or product code using the sidebar.

Tidi Products,Llc is one of 5134 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

Tidi Products,Llc — FDA 510(k) Products and Clearance History

3 devices

1-3 of 3

Data Source

Sourced from the FDA 510(k) public files . 175,143 total devices indexed.

Last updated: Apr 28, 2026