Medical Device Manufacturer · US , Plano , TX

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

6 submissions · 6 cleared · Since 2018

Total

Cleared

Denied

Livermoretech, Inc. has 6 FDA 510(k) cleared medical devices. Based in Plano, US.

Latest FDA clearance: May 2025. Active since 2018. Primary specialty: Radiology.

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

Regulatory submissions have been managed by Mtechgroup, Kamm & Associates and Mtech Group, LLC.

Livermoretech, 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 - Livermoretech, Inc.

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: Apr 29, 2026