Medical Device Manufacturer · US , Salt Lake City , UT

Lumenis Be, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2022

Total

Cleared

Denied

Lumenis Be, Inc. has 1 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.

Last cleared in 2022. Active since 2022. Primary specialty: Ophthalmic.

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

FDA 510(k) cleared devices by Lumenis Be, Inc.

1 devices

1-1 of 1