BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇷 France

    Anthogyr AXIOM® BL X3 implants, Anthogyr Multi-Unit components for AXIOM® BL

    K Number: K230104 · Decision Oct 16, 2023
    View on FDA
    Classifications
    1
    FEI Numbers
    324
    Registration Numbers
    324
    Same Product Code
    1545
    Applicant Total
    10
    Review Days
    276

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    Basic Information

    Device Name
    Anthogyr AXIOM® BL X3 implants, Anthogyr Multi-Unit components for AXIOM® BL
    K Number
    K230104
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    872.3640
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Anthogyr
    Date Received
    January 13, 2023
    Decision Date
    October 16, 2023
    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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