BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

    Clevaligner Software (V1.0.0)

    K Number: K233616 · Decision Jan 11, 2024
    View on FDA
    Classifications
    1
    FEI Numbers
    41
    Registration Numbers
    41
    Same Product Code
    33
    Applicant Total
    1
    Review Days
    59

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    Basic Information

    Device Name
    Clevaligner Software (V1.0.0)
    K Number
    K233616
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    872.5470
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Clevaligner, Ltd.
    Date Received
    November 13, 2023
    Decision Date
    January 11, 2024
    Product Code
    PNN
    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
    PNN Orthodontic Software

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