BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

    InMode VLaze

    K Number: K173677 · Decision Feb 23, 2018
    View on FDA
    Classifications
    1
    FEI Numbers
    476
    Registration Numbers
    479
    Same Product Code
    2793
    Applicant Total
    10
    Review Days
    85

    Basic Information

    Device Name
    InMode VLaze
    K Number
    K173677
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4810
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    InMode MD Ltd.
    Date Received
    November 30, 2017
    Decision Date
    February 23, 2018
    Product Code
    GEX
    Advisory Committee
    General, Plastic Surgery
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    GEX Powered Laser Surgical Instrument

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    Other Clearances by InMode MD Ltd.

    K Number Device Name
    K210492 InMode RF Pro System
    K191855 EmFace Device
    K183450 EmBody System
    K180719 InMode Diolaze System
    K172302 InMode PLUS System
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    K170738 InMode Diolaze XL
    K160329 InMode System MiniFX Handpiece
    K153568 InMode Plus System