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510(k) Data Aggregation

    K Number
    K962277
    Device Name
    SELF CURE BONDING AGENT
    Manufacturer
    DENT ZAR, INC.
    Date Cleared
    1996-07-03

    (20 days)

    Product Code
    KLE
    Regulation Number
    872.3200
    Why did this record match?
    Applicant Name (Manufacturer) :

    DENT ZAR, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
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    K Number
    K960594
    Device Name
    LIGHT SUPER BOND-1 LIGHT CURED ORTHODONTIC ADHESIVE FOR METAL, PLASTIC AND CERAMIC BRACKETS
    Manufacturer
    DENT ZAR, INC.
    Date Cleared
    1996-04-26

    (74 days)

    Product Code
    EBF
    Regulation Number
    872.3690
    Why did this record match?
    Applicant Name (Manufacturer) :

    DENT ZAR, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
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    K Number
    K960595
    Device Name
    FANTASTIC 1 CONTACT CURE ORTHODONTIC ADHESIVE FOR PLASTIC AND METAL BRACKETS
    Manufacturer
    DENT ZAR, INC.
    Date Cleared
    1996-04-26

    (74 days)

    Product Code
    EBF
    Regulation Number
    872.3690
    Why did this record match?
    Applicant Name (Manufacturer) :

    DENT ZAR, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
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    K Number
    K960596
    Device Name
    ORION-I CORE BUILD-UP MATERIAL CHEMICAL CURE
    Manufacturer
    DENT ZAR, INC.
    Date Cleared
    1996-04-26

    (74 days)

    Product Code
    EBF
    Regulation Number
    872.3690
    Why did this record match?
    Applicant Name (Manufacturer) :

    DENT ZAR, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
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    K Number
    K960597
    Device Name
    ORION-1 VL CROWN BASE AND POST CEMENT VISIBLE LIGHT CURE
    Manufacturer
    DENT ZAR, INC.
    Date Cleared
    1996-04-26

    (74 days)

    Product Code
    EBF
    Regulation Number
    872.3690
    Why did this record match?
    Applicant Name (Manufacturer) :

    DENT ZAR, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
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    K Number
    K960598
    Device Name
    CONCORD MARYLAND BRIDGE CEMENT
    Manufacturer
    DENT ZAR, INC.
    Date Cleared
    1996-04-26

    (74 days)

    Product Code
    EBF
    Regulation Number
    872.3690
    Why did this record match?
    Applicant Name (Manufacturer) :

    DENT ZAR, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
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    K Number
    K960599
    Device Name
    SUPERIOR PHOTOCURING HYBRID COMPOSITE
    Manufacturer
    DENT ZAR, INC.
    Date Cleared
    1996-04-26

    (74 days)

    Product Code
    EBF
    Regulation Number
    872.3690
    Why did this record match?
    Applicant Name (Manufacturer) :

    DENT ZAR, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
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    K Number
    K960600
    Device Name
    LEXUR ENAMEL COATING-PORCELAIN REPAIR-BONDING VENEERS
    Manufacturer
    DENT ZAR, INC.
    Date Cleared
    1996-04-26

    (74 days)

    Product Code
    EBF
    Regulation Number
    872.3690
    Why did this record match?
    Applicant Name (Manufacturer) :

    DENT ZAR, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
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    K Number
    K960729
    Device Name
    ENAMEL CONDITIONER (ENAMEL ETCHING AGENT)
    Manufacturer
    DENT ZAR, INC.
    Date Cleared
    1996-04-26

    (64 days)

    Product Code
    EBF
    Regulation Number
    872.3690
    Why did this record match?
    Applicant Name (Manufacturer) :

    DENT ZAR, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
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    K Number
    K960565
    Device Name
    ACORN ANTERIOR/POSTERIOR COMPOSITE RESTORATIVE
    Manufacturer
    DENT ZAR, INC.
    Date Cleared
    1996-03-22

    (42 days)

    Product Code
    EBF
    Regulation Number
    872.3690
    Why did this record match?
    Applicant Name (Manufacturer) :

    DENT ZAR, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
    Ask a Question

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