Lumenis Be, Ltd.

Lumenis Be, Ltd. holds 6 FDA 510(k) medical device clearances, first cleared 2022, most recent 2026.

Top product codes for Lumenis Be, Ltd.

Recent clearances by Lumenis Be, Ltd.

K253803 — MILAN SystemCode GEI·2026-06-02
K250809 — Stellar M22Code GEX·2025-04-16
K242349 — FoLixCode GEX·2024-09-09
K233301 — ULTRApulse Alpha CO2 Laser System, Delivery Devices and AccessoriesCode GEX·2023-12-01
K222790 — F65 Laser SystemCode OAP·2023-06-14
K220467 — The Family of UltraPulse CO2 Surgical and Aesthetic Lasers, Delivery Devices and AccessoriesCode GEX·2022-05-18

Data sourced from openFDA. This site is unofficial and independent of the FDA.