Medical Device Manufacturer · US , Branchburg , NJ

Lifecell Corporation - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2014

Total

Cleared

Denied

Lifecell Corporation has 5 FDA 510(k) cleared medical devices. Based in Branchburg, US.

Historical record: 5 cleared submissions from 2014 to 2020. Primary specialty: General & Plastic Surgery.

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

Lifecell Corporation 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 - Lifecell Corporation

5 devices

1-5 of 5

Data Source

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

Last updated: May 28, 2026