BEUDAMED
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    DePuy Mitek, Inc.

    FDA registration
    DePuy Mitek, Inc.·82 products·🇺🇸 United States

    DEPUY MITEK, INC.

    FDA Adverse Event
    Injury ·DEPUY MITEK·Product code HWC·October 21, 2014

    DEPUY MITEK INC.

    FDA Adverse Event
    Malfunction ·DEPUY MITEK·Product code MLN·December 1, 2010

    UNK - IMPLANT

    FDA Adverse Event
    Injury ·DEPUY MITEK LLC US·Product code HWC·May 18, 2026

    DEPUY MITEK INC OMNISPAN MENISCAL REPAIR SYSTEM

    FDA Adverse Event
    RTI SURGICAL INC·Product code NEW·March 5, 2014

    DePuy Ireland UC

    Authorized representative
    🇮🇪 Ireland·8 Manufacturers

    Orthocord Suture, DePuy Mitek, a Johnson & Johnson Company; . DePuy Mitek, Inc. 325 Paramount Drive, Raynham, MA 02767 Sutures are intended for general soft tissue approximation and/or ligation.

    FDA Recall
    Terminated ·Ethicon, Inc. US·Product code NEW·February 2, 2009

    DePuy Mitek LATARJET EXPERIENCE Extraction Driver Product Code: 288216 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft

    FDA Recall
    Terminated ·DePuy Mitek, Inc., a Johnson & Johnson Co.·Product code HWC·May 12, 2017

    DePuy Mitek LATARJET EXPERIENCE-Combo Screw Driver Product Code: 288211 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft

    FDA Recall
    Terminated ·DePuy Mitek, Inc., a Johnson & Johnson Co.·Product code HWC·May 12, 2017

    DePuy Mitek LATARJET EXPERIENCE Coracoid Drill Product Code: 288201 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft

    FDA Recall
    Terminated ·DePuy Mitek, Inc., a Johnson & Johnson Co.·Product code HWC·May 12, 2017

    DePuy Mitek LATARJET EXPERIENCE Top Hat Tap Product Code: 288203 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft

    FDA Recall
    Terminated ·DePuy Mitek, Inc., a Johnson & Johnson Co.·Product code HWC·May 12, 2017

    DePuy Mitek LATARJET EXPERIENCE Coracoid Top Hat Drill Product Code: 288202 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft

    FDA Recall
    Terminated ·DePuy Mitek, Inc., a Johnson & Johnson Co.·Product code HWC·May 12, 2017

    LATARJET

    FDA Adverse Event
    Injury ·DEPUY MITEK, INC.·Product code HWC·September 24, 2015

    DEPUY MITEK

    FDA Adverse Event
    Injury ·DEPUY MITEK, INC.·Product code MAI·February 17, 2012

    RIGIDFIX FEMORAL ST CROSS PIN KIT

    FDA Adverse Event
    Injury ·DEPUY MITEK, INC.·Product code MBI·January 11, 2012

    VAPR S90ELECTRODE

    FDA Adverse Event
    Malfunction ·DEPUY MITEK INC·Product code GEI·March 22, 2010

    VAPR 90 DEGREE HOOK ELECTRODE

    FDA Adverse Event
    Injury ·DEPUY MITEK, INC.·Product code GEI·January 15, 2010

    MITEK VERSALOK ANCHOR

    FDA Adverse Event
    Malfunction ·DEPUY MITEK, INC.·Product code MBI·May 6, 2010

    UNKNOWN

    FDA Adverse Event
    Malfunction ·DEPUY MITEK, INC.·Product code HWE·November 21, 2017

    EXPRESSEW

    FDA Adverse Event
    Malfunction ·DEPUY/MITEK INC·Product code LXH·August 13, 2015