BEUDAMED
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    AMS COLLAGEN DERMAL MATRIX

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

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306810800·Dean Tonsil Scissors, 18cm

    MEDTRONIC MODEL 7499 EXTENSION

    FDA 510(k)
    FDA Class 2 ·Neurology

    PRECISE NITINOL STENT TRANSHEPATIC BILLARY SYSTEM

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

    PRIMORIS HIP STEM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·August 5, 2016

    BD PHOENIX¿ SMIC-101

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 13, 2026

    PRIMORIS FEMORAL STEM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·October 3, 2017

    PRIMORIS NECK PROSTH BM SZ 26

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·August 4, 2016

    PRIMORIS HIP STEM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·August 5, 2016

    PRMRS NCK STEM TI BM SZ 24 RSA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·June 23, 2016

    MADIGAN ARMY TACOMA WA 1

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA, INC.·Product code DWE·December 7, 2009

    TAPERLOC LAT COCR 10MM T1

    FDA Adverse Event
    Death ·BIOMET UK LTD.·Product code JDI·March 20, 2026

    TPRLOC COCR CMTD STEM T1 7.5MM

    FDA Adverse Event
    Death ·BIOMET UK LTD.·Product code JDI·March 20, 2026

    UNKNOWN PRIMORIS HIP

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·August 4, 2016

    PRMRS NCK STEM TI BM SZ 24 RSA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWY·April 13, 2018

    MARYLAND BIPOLAR FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·April 10, 2013

    TOTALCARE

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·March 15, 2011

    IDENTITY DR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·May 27, 2008

    PRIMORIS NECK PROSTHESIS TI BM SIZE 26

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·November 9, 2017

    UNIV OF VA CHARLOTTESVILLE VA1

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DWF·December 28, 2010