BEUDAMED
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    Gongdong

    FDA UDI
    ZHEJIANG GONGDONG MEDICAL TECHNOLOGY CO., LTD.·06947462492148·face shield, type I

    McKesson

    FDA UDI
    MCKESSON MEDICAL-SURGICAL INC.·00612479258952·Face Shield Full Length 9.5 in

    EX-PRESS MINI GLAUCOMA SHUNT

    FDA Adverse Event
    Malfunction ·OPTONOL, LTD·Product code KYF·April 9, 2014

    EX-PRESS MINI GLAUCOMA SHUNT

    FDA Adverse Event
    Injury ·OPTONOL, LTD·Product code KYF·December 19, 2013

    2.7 VOLT(TM) CRTX/LCKNG DRILL GUIDE FOR 2.0MM DRILL BITS

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code FZX·April 1, 2026

    TRANSSEPTAL NEEDLE, BRK SERIES

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code DRC·January 27, 2026

    EX-PRESS GLAUCOMA FILTRATION DEVICE

    FDA Adverse Event
    Injury ·OPTONOL LTD.·Product code KYF·December 7, 2018

    TRANSSEPTAL NEEDLE, BRK-1 XS SERIES

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code DRC·January 23, 2026

    EX-PRESS GLAUCOMA FILTRATION DEVICE

    FDA Adverse Event
    Injury ·OPTONOL LTD.·Product code KYF·March 29, 2019

    2.7 VOLT(TM) CRTX/LCKNG DRL GD F/2.0 DB

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code FZX·July 29, 2025

    2.7 VOLT(TM) CRTX/LCKNG DRL GD F/2.0 DB

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code FZX·November 21, 2025

    2.7 VOLT(TM) CRTX/LCKNG DRL GD F/2.0 DB

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code FZX·September 15, 2025

    2.7 VOLT(TM) CRTX/LCKNG DRL GD F/2.0 DB

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code FZX·June 17, 2025

    2.0 VOLT(TM) CRTX/LCKNG DRILL GUIDE FOR 1.5MM DRILL BITS

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code FZX·May 27, 2025

    ATEC INTRODUCER LOCALIZATION SET SURESIGHT

    FDA Adverse Event
    Malfunction ·HOLOGIC·Product code GDF·July 1, 2015

    CARB-BITE STERNAL NH 7-3/4

    FDA Adverse Event
    Malfunction ·INTEGRA YORK, PA INC.·Product code GDF·July 16, 2015

    FIXT SUTURING DEVICE

    FDA Adverse Event
    Injury ·BARD SHANNON LIMITED -3005636544·Product code GDF·September 18, 2015

    CODMAN CLASSIC PLUS

    FDA Adverse Event
    Malfunction ·CODMAN·Product code GDF·January 31, 2012

    KARL STORZ

    FDA Adverse Event
    Other ·KARL STORZ GMBH & CO. KG·Product code GDF·January 16, 2009

    UNK

    FDA Adverse Event
    Injury ·UNK·Product code GDF·March 10, 2004