Medical Device Manufacturer · US , Union City , CA

Mizuho America, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1996

Total

Cleared

Denied

Mizuho America, Inc. has 5 FDA 510(k) cleared medical devices. Based in Union City, US.

Last cleared in 2022. Active since 1996. Primary specialty: Neurology.

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

FDA 510(k) cleared devices by Mizuho America, Inc.

5 devices

1-5 of 5