Tidi Products,Llc is one of 5644 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tidi Products,Llc - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
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.
FDA 510(k) Regulatory Record - Tidi Products,Llc
3 devices