Medical Device Manufacturer · US , Pewaukee , WI

Neocoil - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2007

Total

Cleared

Denied

Neocoil has 4 FDA 510(k) cleared medical devices. Based in Pewaukee, US.

Historical record: 4 cleared submissions from 2007 to 2007. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Neocoil Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.

Neocoil is one of 21665 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Neocoil

4 devices

1-4 of 4

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Sep 29, 2026