Medical Device Manufacturer · US , San Jose , CA

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

2 submissions · 2 cleared · Since 2022

Total

Cleared

Denied

Vizaramed, Inc. has 2 FDA 510(k) cleared medical devices. Based in San Jose, US.

Latest FDA clearance: Mar 2026. Active since 2022. Primary specialty: Cardiovascular.

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

Vizaramed, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

2 devices

1-2 of 2