Medical Device Manufacturer · US , Fort Lee , NJ

L&Z Us, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2016

Total

Cleared

Denied

L&Z Us, Inc. has 6 FDA 510(k) cleared medical devices. Based in Fort Lee, US.

Last cleared in 2023. Active since 2016. Primary specialty: General Hospital.

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

L&Z Us, 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 - L&Z Us, Inc.

6 devices

1-6 of 6