BEUDAMED
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    SPROTTE® STANDARD (LUER/ NRFit®) Lumbar Puncture

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Darby Dental Supply, LLC

    FDA UDI
    DARBY DENTAL SUPPLY, LLC·00889813034200·Hedstrom Files with Silicone Stops 31mm #40

    Philips

    FDA UDI
    Sbo Hearing A/S·05714464089796·HEARLINK 1500 MNR BE/TP

    CUSA Clarity Ultrasonic Surgical Aspirator System

    FDA 510(k)
    FDA Unclassified ·Unknown

    LANX ANTERIOR CERVICAL PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LCS COMP RP INSERT STD+ 12.5MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code NJL·December 2, 2008

    MAXPLUS

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code FPA·June 3, 2013

    DAVINCI SURGICAL SYSTEM

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC.·Product code NAY·September 7, 2011

    Azurion 7 M12; Catalog numbers: (1) 722078, (2) 722223, (3) 722233 (OUS ONLY).

    FDA Enforcement
    Class I ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·February 26, 2025

    ACCOLADE DR SL MRI (Model L311)

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025