BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    30K FSI-SLI-1000 INSERT,PKD

    MDR report key: 21513929 · Received March 4, 2025

    Report

    Report Number
    2424472-2025-00209
    Event Type
    Malfunction
    Date Received
    March 4, 2025
    Report Date
    June 6, 2025
    Manufacturer
    DENTSPLY LLC
    Product Code
    ELC
    PMA / PMN Number
    K052334/K970
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AS
    Reporter Occupation
    DENTIST
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    RETURN QTY. (B)(4), 30K FSI-SLI-1000-61, 00130770. WARRANTY PER MANUFACTURE DATE, TEST METHOD / GP005-WI02, INDUCTANCE: GAUGE ID, DUE: (B)(6) 2026, RESULT 3.11, MEETS SPEC, DOES NOT MEET SPEC, N/A. TIP CONDITION: - MEETS SPEC, DOES NOT MEET SPEC, N/A. STACK CONDITION: - MEETS SPEC, DOES NOT MEET SPEC, N/A. TESTED ON: G130 GAGE ID# 9626-2, DUE DATE: (B)(6) 2025, SET PRESSURE: 35 PSI. WATER FLOW: OUTPUT RATE: 35 PSI - MEETS SPEC, DOES NOT MEET SPEC, N/A. SPRAY: - MEETS SPEC, DOES NOT MEET SPEC, N/A. WATER LEAK: HP SEALING RING, PROXIMAL RING, DISTAL RING SEAM LEAK, N/A. VIBRATION: - MEETS SPEC, DOES NOT MEET SPEC, N/A. GRIP CONDITION: MEET, DOES NOT MEET SPEC, N/A. OTHER VISUAL OBSERVATION: INSERT HAS A HP SEALING RING WATER LEAK. INSERT WAS TESTED ON A DIGITAL THERMOMETER I.D.#6116A. DUE DATE: (B)(6) 2025. THE TEMPERATURE WAS 86.9 °F, NO FAULT FOUND. THE SPECIFICATIONS STATE THE TEMPERATURE IS NOT TO EXCEED 118.4°F. (PER FRS-9175 REV 9). ALLEGED EVENT: CONFIRMED, NOT CONFIRMED.

    Additional Manufacturer Narrative · 0

    SINCE AN OVERHEATING INSERT COULD NECESSITATE MEDICAL/SURGICAL INTERVENTION TO PRECLUDE PERMANENT DAMAGE TO A BODY STRUCTURE OR PERMANENT IMPAIRMENT OF A BODY FUNCTION, THIS MALFUNCTION WOULD BE LIKELY TO CAUSE/CONTRIBUTE TO A SERIOUS INJURY SHOULD IT RECUR. AS SUCH, THIS EVENT MEETS THE CRITERIA FOR REPORTABILITY PER 21 CFR PART 803. THE DEVICE IS AVAILABLE FOR EVALUATION, THOUGH HAS NOT BEEN RETURNED AS OF THIS REPORT. EVALUATION RESULTS WILL BE SUBMITTED AS THEY BECOME AVAILABLE.

    Description of Event or Problem · 0

    IN THIS EVENT IT IS REPORTED THAT 30K FSI-SLI-1000 INSERT,PKD ALLEGEDLY THE TIP OVERHEATED DURING USE. NO INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1189339 30K FSI-SLI-1000 INSERT,PKD SCALER, ULTRASONIC ELC DENTSPLY LLC 00130770

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown