Medical Device Manufacturer · US , Minnesota , MN

Interacoustics AS - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2005

Total

Cleared

Denied

Interacoustics AS has 4 FDA 510(k) cleared medical devices. Based in Minnesota, US.

Historical record: 4 cleared submissions from 2005 to 2009. Primary specialty: Ear, Nose, Throat.

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

Interacoustics AS is one of 15041 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Interacoustics AS

4 devices

1-4 of 4

Data Source

Sourced from the FDA 510(k) public files . 175,972 total devices indexed.

Last updated: Sep 25, 2026