Medical Device Manufacturer · US , Wood Dale , IL

Stoelting Co. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1995

Total

Cleared

Denied

Stoelting Co. has 4 FDA 510(k) cleared medical devices. Based in Wood Dale, US.

Historical record: 4 cleared submissions from 1995 to 2001. Primary specialty: Neurology.

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

Stoelting Co. 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 - Stoelting Co.

4 devices

1-4 of 4