BEUDAMED
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    MENTOR DBL-COIL INDWELL. SILICONE URETERAL STENT S

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

    APEX Revision Knee

    FDA UDI
    Omni Life Science, Inc.·00841690111689·Modular Stem 17mm x 150mm

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690117544·Distal Reamer (Hudson)

    HeatLux Pro I

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    SPACELABS MEDICAL MULTIPARAMETER MODULE 91496

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Apex Knee System. Model Numbers: KC-50090, KC-50097, KC-50110, KC-50117, KC-50130, KC-50135, KC-50137, KC-50150, KC-50155, KC-50157, KC-50170, KC-50175, KC-50177, KC-50190, KC-50197, KC-52104, KC-52554, KC-52574, KC-52774, KC-55223, KC-55243

    FDA Enforcement
    Class II ·Ongoing·CORIN MEDICAL, LTD.·July 9, 2025

    TARGET DEVICE GAMMA3® 300X160MM

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL·Product code HSB·June 5, 2014

    SIDEWINDER BLADE ICW

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORPORATION·Product code GEI·November 21, 2012

    HASSON

    FDA Adverse Event
    Malfunction ·ASCENT·Product code GCJ·September 14, 2010

    Apex Knee System. Model Numbers: KC-50090, KC-50097, KC-50110, KC-50117, KC-50130, KC-50135, KC-50137, KC-50150, KC-50155, KC-50157, KC-50170, KC-50175, KC-50177, KC-50190, KC-50197, KC-52104, KC-52554, KC-52574, KC-52774, KC-55223, KC-55243

    FDA Recall
    Open, Classified ·CORIN MEDICAL, LTD. Unit 1-57-8 Corinium Centre Cirencester United Kingdom·Product code JWH·May 23, 2025