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

    Light Cure Composite

    K Number: K240112 · Decision Mar 15, 2024
    View on FDA
    Classifications
    1
    FEI Numbers
    204
    Registration Numbers
    204
    Same Product Code
    931
    Applicant Total
    2
    Review Days
    59

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    Basic Information

    Device Name
    Light Cure Composite
    K Number
    K240112
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    872.3690
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Sincera Technology (Changchun) Co., Ltd.
    Date Received
    January 16, 2024
    Decision Date
    March 15, 2024
    Product Code
    EBF
    Advisory Committee
    Dental
    Review Advisory Committee
    DE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    EBF Material, Tooth Shade, Resin

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    Other Clearances by Sincera Technology (Changchun) Co., Ltd.

    K Number Device Name
    K241056 Light Cure Adhesive