Medical Device Manufacturer · US , Newark , DE

Litecure, LLC - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2007

Total

Cleared

Denied

Litecure, LLC has 7 FDA 510(k) cleared medical devices. Based in Newark, US.

Historical record: 7 cleared submissions from 2007 to 2018. Primary specialty: General & Plastic Surgery.

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

Regulatory submissions have been managed by Intertek Testing Services and Certified Compliance Solutions, Inc..

Litecure, LLC is one of 17568 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Litecure, LLC

7 devices

1-7 of 7

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Jun 08, 2026