BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

    LC GLOSSFILL XR

    K Number: K182778 · Decision Apr 22, 2019
    View on FDA
    Classifications
    1
    FEI Numbers
    204
    Registration Numbers
    204
    Same Product Code
    931
    Applicant Total
    2
    Review Days
    203

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    Basic Information

    Device Name
    LC GLOSSFILL XR
    K Number
    K182778
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    872.3690
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    S&C Polymer Silicon- Und Composite Spezialitaeten GmbH
    Date Received
    October 1, 2018
    Decision Date
    April 22, 2019
    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 S&C Polymer Silicon- Und Composite Spezialitaeten GmbH

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