Medical Device Manufacturer · US , Minneapolis , MN

Nordicneurolab - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2007

Total

Cleared

Denied

Nordicneurolab has 6 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Historical record: 6 cleared submissions from 2007 to 2014. Primary specialty: Radiology.

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

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

Nordicneurolab is one of 18533 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Nordicneurolab

6 devices

1-6 of 6

Data Source

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

Last updated: Sep 18, 2026