BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    SECURIPIN

    K Number: K844457 · Decision Dec 27, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    51
    Registration Numbers
    51
    Same Product Code
    10
    Applicant Total
    1
    Review Days
    41

    Research this 510(k) in seconds

    The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

    Free to try · every answer cites its records

    Ask the Research Assistant See examples

    Basic Information

    Device Name
    SECURIPIN
    K Number
    K844457
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.3740
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Applicant
    Hughes Int'L, Inc.
    Date Received
    November 16, 1984
    Decision Date
    December 27, 1984
    Product Code
    EBL
    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
    EBL Pin, Retentive And Splinting, And Accessory Instruments

    Similar 510(k) Clearances

    Other 510(k) clearances with the same product code (EBL), ordered by most recent decision date.

    CBW BRIDGE SYSTEM (CONSISTING OF CBW ANDCHORS, CBW MICRO-HANDPIECE AND BURS)

    FDA 510(k)
    FDA Class 1 ·Dental

    DENTAURUM JACKET CROWN & ROOT POSTS

    FDA 510(k)
    FDA Class 1 ·Dental

    ROOT CANAL POST

    FDA 510(k)
    FDA Class 1 ·Dental

    PROSTHETIC RESTORATION DEVICE

    FDA 510(k)
    FDA Class 1 ·Dental

    PLASTIC TOOTH REINFORCEMENT KIT

    FDA 510(k)
    FDA Class 1 ·Dental

    ELGILOY

    FDA 510(k)
    FDA Class 1 ·Dental
    View all