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

    Velmeni for Dentists (V4D)

    K Number: K240003 · Decision Aug 30, 2024
    View on FDA
    Classifications
    1
    FEI Numbers
    28
    Registration Numbers
    28
    Same Product Code
    36
    Applicant Total
    3
    Review Days
    241

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    Basic Information

    Device Name
    Velmeni for Dentists (V4D)
    K Number
    K240003
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.2070
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Velmeni, Inc.
    Date Received
    January 2, 2024
    Decision Date
    August 30, 2024
    Product Code
    MYN
    Advisory Committee
    Radiology
    Review Advisory Committee
    RA
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    MYN Analyzer, Medical Image

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    Other Clearances by Velmeni, Inc.

    K Number Device Name
    K252953 Velmeni for Dentists (V4D) Endo-Perio
    K250753 VELMENI for DENTISTS (V4D)