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

    ABSOANCHOR MICROIMPLANT

    K Number: K060126 · Decision May 16, 2006
    View on FDA
    Classifications
    1
    FEI Numbers
    324
    Registration Numbers
    324
    Same Product Code
    1545
    Applicant Total
    2
    Review Days
    118

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    Basic Information

    Device Name
    ABSOANCHOR MICROIMPLANT
    K Number
    K060126
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    872.3640
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Dentos, Inc.
    Date Received
    January 18, 2006
    Decision Date
    May 16, 2006
    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 Dentos, Inc.

    K Number Device Name
    K181142 Absoanchor Microimplant