Medical Device Manufacturer · IL , Yokneam

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

6 submissions · 6 cleared · Since 2022

Total

Cleared

Denied

Lumenis Be, Ltd. has 6 FDA 510(k) cleared medical devices. Based in Yokneam, IL.

Latest FDA clearance: Jun 2026. 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.

Lumenis Be, Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.

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

6 devices

1-6 of 6