BEUDAMED
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    zLOCK Lumbar Facet Fixation System

    FDA 510(k)
    FDA Unclassified ·Unknown

    SpheRx

    FDA UDI
    Nuvasive, Inc.·00887517441874·SpheRx II Screwdriver, Reduction

    Integra® Jarit®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780187196·Integra® Jarit® Bruns Oval Cup Curette, 8", Ang...

    PERSONAL WARMING LUBRICANT

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    UNIVERSA PERCULTANEOUS DRAINAGE CATHETER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    HUDSON OPTI-NEB PRO COMPRESSOR W/DISPOSABLE NE

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code CAF·November 4, 2014

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 9, 2011

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FPO·July 11, 2013

    UNIVERSA LOOP NEPHROSTOMY PERCUTANEOUS DRAINAGE CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code KOB·May 2, 2018

    Model Number L111, ESSENTIO DR SL MRI Pacemaker

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