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Lumenis Be, Ltd.

FDA 510(k) & PMA Approved Devices — 6 products

Total Devices6
Categories3
Latest FDA decision2026-06-02
TypeNumberDevice NameCodeDateActions
510(k) K253803 MILAN SystemGEI2026-06-02 View
510(k) K250809 Stellar M22GEX2025-04-16 View
510(k) K242349 FoLixGEX2024-09-09 View
510(k) K233301 ULTRApulse Alpha CO2 Laser System, Delivery Devices and AccessoriesGEX2023-12-01 View
510(k) K222790 F65 Laser SystemOAP2023-06-14 View
510(k) K220467 The Family of UltraPulse CO2 Surgical and Aesthetic Lasers, Delivery Devices and AccessoriesGEX2022-05-18 View
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