Medical Device Manufacturer · US , Coon Rapids , MN

Endotronics, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1986

Total

Cleared

Denied

Endotronics, Inc. has 3 FDA 510(k) cleared medical devices. Based in Coon Rapids, US.

Historical record: 3 cleared submissions from 1986 to 1988. Primary specialty: Pathology.

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

Endotronics, Inc. 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 - Endotronics, Inc.

3 devices

1-3 of 3