BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

    Injectable Root Canal Bioceramic Sealer (i-MTA SP)

    K Number: K241977 · Decision Oct 3, 2024
    View on FDA
    Classifications
    1
    FEI Numbers
    71
    Registration Numbers
    71
    Same Product Code
    142
    Applicant Total
    2
    Review Days
    90

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    Basic Information

    Device Name
    Injectable Root Canal Bioceramic Sealer (i-MTA SP)
    K Number
    K241977
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    872.3820
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Longly Biotechnology (Wuhan) Co., Ltd.
    Date Received
    July 5, 2024
    Decision Date
    October 3, 2024
    Product Code
    KIF
    Advisory Committee
    Dental
    Review Advisory Committee
    DE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    KIF Resin, Root Canal Filling

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    Other Clearances by Longly Biotechnology (Wuhan) Co., Ltd.

    K Number Device Name
    K242934 Bioceramic Root Canal Sealer and Repair Materials (i-MTA BP)