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510(k) Data Aggregation

    K Number
    K092583
    Device Name
    SOPROLIFE
    Manufacturer
    Date Cleared
    2010-01-13

    (145 days)

    Product Code
    Regulation Number
    872.1745
    Panel
    Dental
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    SOPROLIFE

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The SOPROLIFE is indicated as an aid in the diagnosis of dental caries and as an intra oral camera to visualize anatomical details invisible to the naked eye or with mirror.

    Device Description

    The SOPROLIFE is a fluorescence caries detection device . This device is a fluorescence detector housed in a dental handpiece, and a control unit that performs device calibration, as well as variable tone emitting and fluorescence measurement functions.
    The handbiece can be connected with 5 different control units : Dock M VIDEO Dock M USB2. Dock MU VIDEO, Dock MU USB2, Dock USB2.
    The SOPROLIFE is a device used in clinical dental applications to observe the condition of hard dentinal tissues.
    As the SOPROLIFE can be adapted to the most complex of clinical situations, it quickly helps the dentist to get a complete analysis as it adjusts treatment options in Diagnosis aid mode. In Treatment aid mode, the SOPROLIFE facilitates observation of the dentinal tissue condition in progress and at the end of the treatment. In daylight mode the SOPROLIFE enables the dentist to visualize anatomical details invisible to the naked eye or with mirror like an intra oral camera SOPRO 595.

    AI/ML Overview

    This document is a 510(k) summary for the SOPROLIFE device, a fluorescence caries detection device. It outlines the device description, intended use, indications for use, and a comparison to predicate devices, but it does not contain information about acceptance criteria or a study proving the device meets acceptance criteria.

    Therefore, I cannot extract the requested information from the provided text. The document is primarily a regulatory submission for premarket notification, establishing substantial equivalence to existing devices rather than detailing the results of performance studies against specific acceptance criteria.

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