BEUDAMED
    FDA 510(k) FDA unclassified Substantially Equivalent 🇯🇵 Japan

    NailLift

    K Number: K230841 · Decision Jan 22, 2024
    View on FDA
    Classifications
    1
    FEI Numbers
    1
    Registration Numbers
    1
    Same Product Code
    3
    Applicant Total
    1
    Review Days
    300

    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
    NailLift
    K Number
    K230841
    Device Class
    FDA unclassified
    Clearance Type
    Traditional
    Medical Specialty
    Unknown
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Jps Corporation
    Date Received
    March 28, 2023
    Decision Date
    January 22, 2024
    Product Code
    MQZ
    Advisory Committee
    Unknown
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

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

    Product Code Device Name
    MQZ Prosthesis, Nail

    Similar 510(k) Clearances

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

    Oniko nail brace

    FDA 510(k)
    FDA Unclassified ·Unknown

    STOP-N-GROW

    FDA 510(k)
    FDA Unclassified ·Unknown

    NAIL SPLINT

    FDA 510(k)
    FDA Unclassified ·Unknown
    View all