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510(k) Data Aggregation

    K Number
    K121915
    Manufacturer
    Date Cleared
    2012-09-28

    (88 days)

    Product Code
    Regulation Number
    872.3690
    Panel
    Dental
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    BRIGHT Restorative Materials, to include:

    • NANOCERAM BRIGHT FLOW .
    • BRIGHT FLOW CORE .
    • BRIGHT HEAVY CORE .
    • BRIGHT LIGHT .
    • BRIGHT LIGHT FLOW .
    • · BRIGHT POSTERIOR

    Indications for Use:

    NANOCERAM - BRIGHT FLOW
    Indications for use:

    • · Fillings of minimally invasive cavities of all classes
    • Fillings of small class I cavities .
    • Fillings of class II-V cavities including V-shaped defects and cervical caries
    • Extended fissure sealing
    • Cavity lining as the first layer for Class I and II restorations
    • Splinting of mobile teeth ●
    • Blocking out of undercuts
    • Small restorations of all types
    • Repair of composite restorations and ceramic veneers

    BRIGHT FLOW CORE - BRIGHT HEAVY CORE
    Indications for use:

    • Core build up of vital and non-vital teeth .
    • Post cementation

    BRIGHT LIGHT - BRIGHT LIGHT FLOW
    BRIGHT LIGHT
    Indications for use:

    • Class I-V restorations .
    • Reconstruction of affected anterior teeth ●
    • Veneering of discoloured anterior teeth .
    • Splinting of mobile teeth
    • Repair of composite and ceramic veneers

    BRIGHT LIGHT FLOW
    Indications for use:

    • · Fillings of minimally invasive cavities of all classes
    • Fillings of class II-V cavities including V-shaped defects and cervical caries .
    • Extended fissure sealing .
    • Splinting of mobile teeth .
    • Blocking out of undercuts .
    • Small restorations of all types .
    • Repair of composite restorations and ceramic veneers

    BRIGHT POSTERIOR
    Indications for use:

    • · Direct posterior restorations (Class I and II), including occlusal surfaces
    • Core build ups ●
    • Splinting of mobile teeth
    Device Description

    Not Found

    AI/ML Overview

    The provided documentdoes not contain information about acceptance criteria or a study proving device performance against such criteria.

    The document is a 510(k) premarket notification letter from the FDA to DMP. Limited regarding their "Bright Restorative Materials". It states that the device has been determined to be substantially equivalent to legally marketed predicate devices.

    The content primarily focuses on:

    • The FDA's determination of substantial equivalence.
    • Regulatory information and obligations for the manufacturer.
    • Indications for use for various Bright Restorative Materials.

    Therefore, I cannot provide the requested information, including the table of acceptance criteria, sample sizes, ground truth details, or information about MRMC studies.

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