Lumenis Be, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K250809Stellar M22April 16, 2025
K242349FoLixSeptember 9, 2024
K233301ULTRApulse Alpha CO2 Laser System, Delivery Devices and AccessoriesDecember 1, 2023
K222790F65 Laser SystemJune 14, 2023
K220877Selecta Duet LED, Digital Duet, Selecta LED Trio, Digital Trio Laser SystemsJuly 15, 2022
K220467The Family of UltraPulse CO2 Surgical and Aesthetic Lasers, Delivery Devices and AccessoriesMay 18, 2022