BEUDAMED
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    LANX FACET SCREW SYSTEM

    FDA 510(k)
    FDA Unclassified ·Unknown

    Bur PM2-70 80K diamC Ø3.1 St

    FDA UDI
    Bien-Air Surgery SA·17630055517095·

    Preci-Sagix

    FDA UDI
    Preat Corporation·00842092108840·Sagix 2.2 Female Combo Pack Includes: 2 (yellow...

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517573698·CoRoent Ant TLIF Ti, 10x11x36mm 4°

    ILIZAROV

    FDA UDI
    Smith & Nephew, Inc.·03596010030542·5/8 RING 150MM COMPOSITE

    CUSTOM TCI (TINNITUS CONTROL INSTRUMENT)

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    BD DIRECTIGEN FLU A+B

    FDA 510(k)
    FDA Class 2 ·Microbiology

    ADVANIX BILIARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·January 8, 2025

    KYPHOPAK TRAY

    FDA Adverse Event
    Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code HRX·May 24, 2021

    ADVANIX BILIARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·December 5, 2024

    KYPHON XPANDER II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO·Product code HRX·November 6, 2019

    KYPHON XPANDER II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO·Product code HRX·April 5, 2021

    KYPHON XPANDER II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO·Product code HRX·July 11, 2019

    KYPHON XPANDER II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO·Product code HRX·August 31, 2019

    KYPHON XPANDER II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code HRX·March 7, 2018

    PRESOURCE CRANIOTOMY PACK

    FDA Adverse Event
    Malfunction ·CARDINAL·Product code LRP·May 19, 2011

    SUTURE ANCH BIOCOMP SWIV SP, SELF-PUN 4.75X24.5MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code MAI·May 9, 2013

    GRANUFLO

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·September 3, 2014

    KYPHON XPANDER II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code HRX·May 17, 2018

    1030489-2019-01511

    FDA Adverse Event
    Death ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NDN·December 31, 2019