Medical Device Manufacturer · US , Houston , TX

Honeywell Hommed, LLC - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2006

Total

Cleared

Denied

Honeywell Hommed, LLC has 7 FDA 510(k) cleared medical devices. Based in Houston, US.

Historical record: 7 cleared submissions from 2006 to 2016. Primary specialty: Cardiovascular.

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

510(k) submissions have been managed by Spectramedex, LLC as regulatory consultant.

Honeywell Hommed, LLC is one of 13019 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Honeywell Hommed, LLC

7 devices

1-7 of 7

Data Source

Sourced from the FDA 510(k) public files . 175,972 total devices indexed.

Last updated: Sep 16, 2026