Medical Device Manufacturer · US , Grand Rapids , MI

Nordex Medical Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1993

Total

Cleared

Denied

Nordex Medical Corp. has 2 FDA 510(k) cleared medical devices. Based in Grand Rapids, US.

Historical record: 2 cleared submissions from 1993 to 1994. Primary specialty: General Hospital.

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

Nordex Medical Corp. 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 - Nordex Medical Corp.

2 devices

1-2 of 2