BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    NEODENT IMPLANT SYSTEM

    K Number: K101945 · Decision Jan 26, 2011
    View on FDA
    Classifications
    1
    FEI Numbers
    333
    Registration Numbers
    333
    Same Product Code
    1516
    Applicant Total
    11
    Review Days
    198

    Basic Information

    Device Name
    NEODENT IMPLANT SYSTEM
    K Number
    K101945
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    872.3640
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    JJGC INDUSTRIA E COMERCIO DE MATERIAIS DENTARIOS S
    Date Received
    July 12, 2010
    Decision Date
    January 26, 2011
    Product Code
    DZE
    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
    DZE Implant, Endosseous, Root-Form

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    Other Clearances by JJGC INDUSTRIA E COMERCIO DE MATERIAIS DENTARIOS S

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