BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

    Q-Switched Nd: YAG Laser System (Glamor Q)

    K Number: K260153 · Decision Apr 20, 2026
    View on FDA
    Classifications
    1
    FEI Numbers
    478
    Registration Numbers
    480
    Same Product Code
    2867
    Applicant Total
    5
    Review Days
    90

    Basic Information

    Device Name
    Q-Switched Nd: YAG Laser System (Glamor Q)
    K Number
    K260153
    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
    Nanjing Bestview Laser S&T Co., Ltd.
    Date Received
    January 20, 2026
    Decision Date
    April 20, 2026
    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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