BEUDAMED
    FDA Registration Active 🇺🇸 United States

    M22 ResurFX module

    Reg #: 1720381 · FEI: 1720381 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    8
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    LUMENIS, INC.
    Registration Number
    1720381
    FEI Number
    1720381
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    1870 S Milestone Dr
    City
    SALT LAKE CITY
    State
    UT
    ZIP
    84104
    Country
    US

    Owner / Operator

    Firm Name
    Lumenis Be LTD
    Operator Number
    9017014
    Address
    9 Hakidma St., POB 426, Yokneam Industrial Park
    City
    Yokneam
    State
    IL-NOTA
    Postal Code
    2069236
    Country
    IL

    Products

    Device Name Product Code
    Powered Laser Surgical Instrument With MicrobeamFractional Output ONG

    Proprietary Names

    M22 ResurFX module M22 IPL handpiece IPL LightGuides IPL Filters M22 Q-Switched module Acne Filter M22 IPL and Nd:YAG module Vascular Filter

    Establishment Types

    Manufacture Device in the United States for Export Only