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

    LUSTRE GoGlow Advanced LED Patches (PR8001, PR9001)

    K Number: K253878 · Decision Mar 4, 2026
    View on FDA
    Classifications
    1
    FEI Numbers
    109
    Registration Numbers
    109
    Same Product Code
    50
    Applicant Total
    23
    Review Days
    90

    Basic Information

    Device Name
    LUSTRE GoGlow Advanced LED Patches (PR8001, PR9001)
    K Number
    K253878
    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
    Shenzhen Kaiyan Medical Equipment Co., Ltd.
    Date Received
    December 4, 2025
    Decision Date
    March 4, 2026
    Product Code
    OLP
    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
    OLP Over-The-Counter Powered Light Based Laser For Acne

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