Medical Device Manufacturer · US , Stamford , CT

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

5 submissions · 5 cleared · Since 2001

Total

Cleared

Denied

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

Latest FDA clearance: Dec 2024. Active since 2001. Primary specialty: Ear, Nose, Throat.

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

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

Vivosonic, Inc. is one of 16052 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

5 devices

1-5 of 5

Data Source

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

Last updated: May 10, 2026