BEUDAMED
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    MODIFICATION TO OUTBACK CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    WRIGHT MEDICAL TECHNOLOGY, INC.

    FDA registration
    WRIGHT MEDICAL TECHNOLOGY, INC.·93 products·🇺🇸 United States

    PENTRA 5D

    FDA 510(k)
    FDA Class 2 ·Hematology

    SELF-COUNTERSINKING BONE SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    1043534-2012-01254

    FDA Adverse Event
    Malfunction ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LWJ·October 2, 2012

    1043534-2011-00074

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC·May 1, 2012

    1043534-2012-00125

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC·May 10, 2012

    1043534-2012-00126

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC·May 10, 2012

    1043534-2012-01258

    FDA Adverse Event
    Malfunction ·WRIGHT MEDICAL TECHNOLOGY, INC.·November 29, 2012

    1043534-2010-00457

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC·July 28, 2011

    1043534-1997-00006

    FDA Adverse Event
    Product code JWH·September 2, 1997

    1043534-2012-01253

    FDA Adverse Event
    Malfunction ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LWJ·October 2, 2012

    1043534-2012-01259

    FDA Adverse Event
    Malfunction ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code MAY·October 2, 2012

    1043534-2012-01252

    FDA Adverse Event
    Malfunction ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LWJ·October 2, 2012

    1043534-2012-00513

    FDA Adverse Event
    Malfunction ·WRIGHT MEDICAL TECHNOLOGY, INC.·October 15, 2012

    1043534-2012-01250

    FDA Adverse Event
    Malfunction ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LWJ·October 2, 2012

    1043534-2012-01251

    FDA Adverse Event
    Malfunction ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code JWH·October 2, 2012

    1043534-2012-01257

    FDA Adverse Event
    Malfunction ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LPH·October 2, 2012

    1043534-2012-01176

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·November 29, 2012

    1043534-2012-01255

    FDA Adverse Event
    Malfunction ·WRIGHT MEDICAL TECHNOLOGY, INC.·October 2, 2012