Medical Device Manufacturer · US , Minneapolis , MN

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

5 submissions · 5 cleared · Since 2013

Total

Cleared

Denied

Intervalve, Inc. has 5 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Historical record: 5 cleared submissions from 2013 to 2015. Primary specialty: Cardiovascular.

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

510(k) submissions have been managed by Libramedical, Inc. as regulatory consultant.

Intervalve, Inc. is one of 19600 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

5 devices

1-5 of 5

Data Source

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

Last updated: Sep 18, 2026