BEUDAMED
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    KAR

    FDA UDI
    DEPUY FRANCE·10603295260684·KAR Cementless Revision Femoral Stem with Colla...

    KAR

    FDA UDI
    DEPUY FRANCE·10603295260660·KAR Cementless Revision Femoral Stem with Colla...

    KAR

    FDA UDI
    DEPUY FRANCE·10603295260677·KAR Cementless Revision Femoral Stem with Colla...

    DEPUY FRANCE CORAIL

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWA·March 26, 2013

    UNKNOWN DEPUY FRS SCREW

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code HWC·February 26, 2010

    UNKNOWN DEPUY FRS SCREW

    FDA Adverse Event
    Injury ·DEPUY ACE S.A. 'R.L.·Product code HWC·December 30, 2009

    UNKNOWN DEPUY FRS SCREW

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code HWC·August 1, 2006

    STANDARD METAGLENE V3.2

    FDA Adverse Event
    Injury ·DEPUY FRANCE S.A.·Product code KWS·April 2, 2009

    PFC MODULAR KNEE SYSTEM CURVED TIBIAL INSERT

    FDA Adverse Event
    Malfunction ·DEPUY-RAYNHAM, A DIVISION OF DEPUY ORTHOPAEDICS, INC.·Product code JWH·October 23, 2001

    PFC TOTAL KNEE SYSTEM OVAL PATELLA

    FDA Adverse Event
    Malfunction ·DEPUY-RAYNHAM, A DIVISION OF DEPUY ORTHOPAEDICS, INC.·Product code JWH·October 23, 2001

    DELTA CTD HUM EPI.42.2

    FDA Adverse Event
    Injury ·DEPUY FRANCE·Product code KWS·May 15, 2012

    GLENOSPHERE ORIENTATION GUIDE

    FDA Adverse Event
    Malfunction ·DEPUY FRANCE SAS 3003895575·Product code LXH·June 9, 2014

    DXTEND METAGLENE

    FDA Adverse Event
    Injury ·DEPUY FRANCE, S.A.·Product code HSD·August 17, 2011

    DXTEND MOD EPI 1 ECC RIGHT HA

    FDA Adverse Event
    Injury ·DEPUY FRANCE S.A.S. -SAINT PRIEST·Product code KWS·March 10, 2011

    DXTEND SCREW NO LOCK D4.5X18MM

    FDA Adverse Event
    Injury ·3003895575 DEPUY FRANCE S.A.S.-SAINT PRIEST·Product code HSD·September 4, 2013

    DXTEND STAND PE CUP D38 +6MM

    FDA Adverse Event
    Injury ·3003895575 DEPUY FRANCE S.A.S.-SAINT PRIEST·Product code KWS·September 4, 2013

    DXTEND SCREW LOCK D4.5X30MM

    FDA Adverse Event
    Injury ·3003895575 DEPUY FRANCE S.A.S.-SAINT PRIEST·Product code HSD·September 4, 2013

    DXTEND SCREW NO LOCK D4.5X24MM

    FDA Adverse Event
    Injury ·3003895575 DEPUY FRANCE S.A.S.-SAINT PRIEST·Product code HSD·September 4, 2013

    DXTEND METAGLENE

    FDA Adverse Event
    Injury ·3003895575 DEPUY FRANCE S.A.S.-SAINT PRIEST·Product code HSD·September 4, 2013

    DXTEND GLENOSPHERE STD D38MM

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWS·December 3, 2015