BEUDAMED
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    ADVIA CENTAUR AND ACS:180 LIQUID CARDIAC MARKERS 1, 2, 3

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Tornier Latitude

    FDA UDI
    TORNIER, INC.·00846832015047·HUMERAL REVISION STEM TRIAL

    LOCATOR R-Tx

    FDA UDI
    Zest Anchors, LLC·00840481110283·LOCATOR R-Tx Abument for 4.5 Internal Hex Conne...

    Humelock Reversed Shoulder

    FDA UDI
    FX SOLUTIONS·03701037306185·HUMELOCK REVERSED T HANDLE / AO

    RHEAD

    FDA UDI
    Stryker GmbH·00886385003702·Neck Plate, Fixed Angle Locking, Standard

    LOCATOR F-Tx

    FDA UDI
    Zest Anchors, LLC·00840481114236·LOCATOR F-Tx Abutment for 4.1mm Certain Interna...

    Discectomy Set

    FDA UDI
    SPINEOLOGY INC.·M7403030102·8mm Shaver

    LOCATOR R-Tx

    FDA UDI
    Zest Anchors, LLC·00840481128233·LOCATOR R-Tx Abutment, 4.1mm Certain Connection...

    LIF-PTP

    FDA UDI
    ALPHATEC SPINE, INC.·00190376284101·Paddle Assembly, Thoracic, Right, LIF-PTP

    LIF-PTP

    FDA UDI
    ALPHATEC SPINE, INC.·00190376284095·Paddle Assembly, Thoracic, Left, LIF-PTP

    GLUCOSE (HEXOKINASE) LIQUID REAGENT, MODEL G518-150

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    PARE ENDOSCOPIC SUTURING SYSTEM

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

    ACCU-CHEK SPIRIT COMBO

    FDA Adverse Event
    Malfunction ·ROCHE DIABETES CARE AG·Product code LZG·April 2, 2013

    HERCULES 3 STAGE WIREGUIDED BALLOON ESOPHAGEAL PYLORIC-COLONIC

    FDA Adverse Event
    Malfunction ·WILSON-COOK MEDICAL INC.·Product code KNQ·July 30, 2014

    LOCKING TITANIUM ADAPTER

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SWINFORD·Product code KDJ·March 26, 2011

    PROGRASP FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·December 2, 2013

    PLUM LS PRIM. 225 CM CLAVE PORT DISTA

    FDA Adverse Event
    Injury ·HOSPIRA COSTA RICA LTD.·Product code FPA·March 22, 2013

    PERFUSOR SPACE

    FDA Adverse Event
    Malfunction ·B.BRAUN MELSUNGEN AG·Product code FRN·October 1, 2022

    Sample Management System software for in vitro diagnostic testing Product # 030102-03

    FDA Recall
    Terminated ·Siemens Medical Solutions Diagnostics·Product code CDD·January 15, 2007

    ASSEMBLY-ROTARY SCALE: 190-00126

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code OLO·January 2, 2019