Medical Device Manufacturer · US , Bothell , WA

Verathon Incorporated - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2007

Total

Cleared

Denied

Verathon Incorporated has 5 FDA 510(k) cleared medical devices. Based in Bothell, US.

Historical record: 5 cleared submissions from 2007 to 2017. Primary specialty: Radiology.

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

510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.

Verathon Incorporated is one of 13692 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Verathon Incorporated

5 devices

1-5 of 5

Data Source

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

Last updated: Sep 14, 2026