BEUDAMED
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    KENDALL SCD 700 SEQUENTIAL COMPRESSION CONTROLLER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517574763·CoRoent Ant TLIF Ti, 13x12x36mm 0°

    PIVOX™ Oblique Lateral Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169605961·SPACER 2132360 OLIF25 27MM 12 DEG 12X60

    HHM

    FDA UDI
    Oticon A/S·05707131258182·H160, RITE 312 WL TC HHM

    Olsen Webster Needle Holder

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896116962·Olsen Webster Needle Holder Tungsten Carbide Sm...

    Ophthalmic Spatula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668102602·LIEBERMAN MICROFINGER RIGHT

    ICESENCE 3

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MODIFICATION TO BOSTON SCIENTIFIC EXPRESS BILIARY LD PREMOUNTED STENT SYSTEM AND EXPRESS BILIARY LD UNMOUNTED STENT

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

    AXOGUARD NERVE CONNECTOR AND PROTECTOR

    FDA Adverse Event
    Injury ·COOK BIOTECH·Product code JXI·August 24, 2015

    BE-PLS 2050

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·February 26, 2014

    BE-PLS 2050 PERMENANT LIFE SUPPORT

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code KFM·March 6, 2014

    BE-PLS 2050 PERMENANT LIFE SUPPORT

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·February 27, 2014

    HLS SET

    FDA Adverse Event
    Death ·MAQUET CARDIOPULMONARY GMBH·Product code DTZ·August 18, 2025

    TUBING SET

    FDA Adverse Event
    Death ·MAQUET CARDIOPULMONARY GMBH·Product code DTZ·April 28, 2025

    TUBING SET

    FDA Adverse Event
    Death ·MAQUET CARDIOPULMONARY GMBH·Product code DTZ·April 28, 2025

    TUBING SET

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTZ·January 20, 2026

    TUBING SET

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTZ·January 20, 2026

    ASR XL TAP SLV ADAP 12/14+8

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·May 29, 2013

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code LWS·October 1, 2014

    CONTOUR TEST STRIPS

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE, LLC·Product code NBW·June 13, 2011