Medical Device Manufacturer · US , Stoughton , WI

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

3 submissions · 3 cleared · Since 2005

Total

Cleared

Denied

Inntec, Inc. has 3 FDA 510(k) cleared medical devices. Based in Stoughton, US.

Historical record: 3 cleared submissions from 2005 to 2005. Primary specialty: Obstetrics & Gynecology.

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

Inntec, Inc. is one of 23753 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Inntec, Inc.

3 devices

1-3 of 3