Medical Device Manufacturer · CA , Burnaby

Verathon Medical (Canada) Ulc - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2019

Total

Cleared

Denied

Verathon Medical (Canada) Ulc has 6 FDA 510(k) cleared medical devices. Based in Burnaby, CA.

Latest FDA clearance: May 2026. Active since 2019. Primary specialty: Ear, Nose, Throat.

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

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

Verathon Medical (Canada) Ulc is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Verathon Medical (Canada) Ulc

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: Jun 05, 2026