BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

    Laon Ortho

    K Number: K250198 · Decision Apr 23, 2025
    View on FDA
    Classifications
    1
    FEI Numbers
    41
    Registration Numbers
    41
    Same Product Code
    33
    Applicant Total
    2
    Review Days
    90

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    Basic Information

    Device Name
    Laon Ortho
    K Number
    K250198
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    872.5470
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Laon Medi, Inc.
    Date Received
    January 23, 2025
    Decision Date
    April 23, 2025
    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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    Other Clearances by Laon Medi, Inc.

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