Lumenis Be, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lumenis Be, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Selecta Duet LED, Digital Duet, Selecta LED Trio, Digital Trio Laser Systems
1
Total
1
Cleared
0
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) Regulatory Record - Lumenis Be, Inc.
1 devices