BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

    Pentacam® Cornea OCT

    K Number: K251848 · Decision Mar 13, 2026
    View on FDA
    Classifications
    1
    FEI Numbers
    18
    Registration Numbers
    18
    Same Product Code
    22
    Applicant Total
    2
    Review Days
    270

    Basic Information

    Device Name
    Pentacam® Cornea OCT
    K Number
    K251848
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    886.1850
    Medical Specialty
    Ophthalmic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Oculus Optikgeräte GmbH
    Date Received
    June 16, 2025
    Decision Date
    March 13, 2026
    Product Code
    MXK
    Advisory Committee
    Ophthalmic
    Review Advisory Committee
    OP
    Third Party
    N

    Classifications

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

    Product Code Device Name
    MXK Device, Analysis, Anterior Segment

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