Medical Device Manufacturer · US , St Louis , MO

Hi-Dow International, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2011

Total

Cleared

Denied

Hi-Dow International, Inc. has 6 FDA 510(k) cleared medical devices. Based in St Louis, US.

Latest FDA clearance: Jan 2024. Active since 2011. Primary specialty: Neurology.

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

Hi-Dow International, 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 - Hi-Dow International, Inc.

6 devices

1-6 of 6