FDA 510(k) Applications Submitted by Shlomit Segman

FDA 510(k) Number Submission Date Device Name Applicant
K140381 02/14/2014 SENSILIGHT/ SENSILIGHT PLUS EL GLOBAL TRADE LTD.
K220467 02/17/2022 The Family of UltraPulse CO2 Surgical and Aesthetic Lasers, Delivery Devices and Accessories Lumenis Be, Ltd.
K140527 03/04/2014 SENSILIGHT MINI EL GLOBAL TRADE LTD.
K220877 03/25/2022 Selecta Duet LED, Digital Duet, Selecta LED Trio, Digital Trio Laser Systems Lumenis Be, Inc.
DEN200028 04/20/2020 Lumenis Stellar M22 Lumenis Ltd.
K201663 06/19/2020 AcuPulse W CO2 Laser Systems, Delivery Devices and Accessories Lumenis Ltd.
K202428 08/25/2020 AcuPulse W CO2 Laser Systems, Delivery Devices and Accessories Lumenis Ltd.
K212703 08/26/2021 AcuPulse CO2 Laser System, Delivery Devices and Accessories Lumenis, Ltd.
K222790 09/15/2022 F65 Laser System Lumenis Be, Ltd.
K203544 12/04/2020 UltraPulse Surgical and Aesthetic CO2 Laser System, Delivery Devices and Accessories Lumenis Ltd.
K193500 12/17/2019 Stellar M22 for Intense Pulsed Light (IPL) and Laser System Lumenis Ltd.


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