Medical Device Manufacturer · US , Mchenry , IL

Hemometrix - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1979

Total

Cleared

Denied

Hemometrix has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 7 cleared submissions from 1979 to 1980. Primary specialty: Toxicology.

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

Hemometrix 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 - Hemometrix

7 devices

1-7 of 7

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: Apr 27, 2026