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    ARTHREX, INC.

    FDA Adverse Event
    Malfunction ·BOVIE MEDICAL CORPORATION·Product code GEI·November 18, 2014

    ARTHREX INC.

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MBI·December 27, 2003

    ARTHREX, INC.

    FDA Adverse Event
    Malfunction ·BOVIE MEDICAL CORPORATION·Product code GEI·September 28, 2011

    ARTHREX INC.

    FDA Adverse Event
    Injury ·ARTHREX INC.·Product code HRY·July 30, 1998

    ARTHREX, INC

    FDA Adverse Event
    Injury ·ARTHREX, INC·Product code HTN·November 13, 2007

    ARTHREX, INC.

    FDA Adverse Event
    Other ·ARTHREX, INC.·Product code MAI·June 9, 2003

    ARTHREX INC.

    FDA Adverse Event
    Other ·ARTHREX, INC.·Product code MAI·June 9, 2003

    ARTHREX, INC

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code FMI·December 29, 2011

    ARTHREX, INC

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code GAB·December 29, 2011

    ARTHREX, INC.

    FDA Adverse Event
    Injury ·BOVIE MEDICAL CORPORATION·Product code GEI·September 5, 2013

    ARTHREX, INC.

    FDA Adverse Event
    Other ·ARTHREX, INC.·Product code MAI·June 12, 2002

    ARTHREX, INC.

    FDA Adverse Event
    Other ·ARTHREX, INC.·Product code HRS·June 12, 2002

    ARTHREX, INC.

    FDA Adverse Event
    Malfunction ·ARTHREX INC.·Product code HRX·September 8, 2006

    ARTHREX, INC

    FDA Adverse Event
    Injury ·BOVIE MEDICAL CORPORATION·Product code GEI·March 13, 2015

    ARTHREX, INC. SCORPION NEEDLE, KNEE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MDM·January 2, 2024

    ACL TIGHTROPE RT- ARTHREX INC.

    FDA Adverse Event
    Injury ·ARTHREX·Product code HTY·January 21, 2016

    ARTHREX INC SCORPION MULTIFIRE NEEDLE

    FDA Adverse Event
    Malfunction ·ARTHREX INC.·Product code GAB·September 13, 2018

    NANOSCOPE CONSOLE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code GCJ·June 11, 2024

    NANOSCOPE CONSOLE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code GCJ·April 24, 2024

    OSFERION

    FDA Adverse Event
    Injury ·OSFERIONBIOMATERIALS CORP. MISHIMA FACTORY·Product code MQV·April 28, 2026