Medical Device Manufacturer · IL , Yokneam

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

5 submissions · 5 cleared · Since 2022

Total

Cleared

Denied

Lumenis Be, Ltd. has 5 FDA 510(k) cleared medical devices. Based in Yokneam, IL.

Latest FDA clearance: Apr 2025. Active since 2022. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) Regulatory Record - Lumenis Be, Ltd.

5 devices

1-5 of 5

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: May 02, 2026