BEUDAMED
    214 results · 34ms · Sources: EU EUDAMED, US FDA

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    VITEK INC.

    FDA Adverse Event
    Injury ·VITEK, INC.·Product code JAZ·November 30, 2009

    VITEK, INC.

    FDA Adverse Event
    Injury ·VITEK, INC.·Product code LZD·November 30, 2009

    VITEK INC.

    FDA Adverse Event
    Injury ·VITEK INC.·Product code LZD·September 30, 2004

    VITEK INC.

    FDA Adverse Event
    Death ·VITEK INC.·Product code LZD·June 18, 2004

    VITEK INC

    FDA Adverse Event
    Injury ·VITEK, INC (NO LONGER IN BUSINESS)·Product code LZD·April 4, 2008

    VITEK PROPLAST TMJ IMPLANT

    FDA Adverse Event
    Injury ·VITEK, INC.·Product code LZD·April 17, 1992

    VITEK PROPLAST TMJ IMPLANT

    FDA Adverse Event
    Injury ·VITEK, INC·Product code LZD·May 21, 1992

    PROPLAST TEFLON MANDIBULAR IMPLANT

    FDA Adverse Event
    Injury ·VITEK, INC.·Product code LZD·August 29, 1996

    METAL TMJ IMPLANT

    FDA Adverse Event
    Injury ·VITEK, INC.·Product code LZD·August 28, 1996

    VITEK IPI

    FDA Adverse Event
    Injury ·VITEK, INC.·Product code LZD·May 31, 2012

    PROPLAST TEFLON TMJ IMPLANT

    FDA Adverse Event
    Injury ·VITEK, INC.·Product code LZD·May 13, 1996

    VITEK IMPLANTS

    FDA Adverse Event
    Other ·VITEK, INC·Product code LZD·July 11, 2000

    TMJ PROPLAST PROSTHESIS

    FDA Adverse Event
    VITEK, INC.·Product code LZD·February 1, 1994

    TMJ IMPLANT

    FDA Adverse Event
    Injury ·VITEK, INC.·Product code LZD·March 23, 1994

    PROPLAST TEFLON TMJ FOSSA IMPLANT

    FDA Adverse Event
    Other ·VITEK, INC.·Product code LZD·January 10, 1994

    VITEK GLENOID FOSSA IMPLANT

    FDA Adverse Event
    Injury ·VITEK, INC.·Product code MDL·February 2, 1994

    PROPLAST TEFLON IMPLANT

    FDA Adverse Event
    Injury ·VITEK, INC.·Product code LZD·January 21, 1994

    PROPLAST

    FDA Adverse Event
    Malfunction ·VITEK, INC.·Product code LZD·March 17, 1994

    INTERPOSITIONAL TMJ TEFLON PROPLAST IMPLANT

    FDA Adverse Event
    Injury ·VITEK, INC.·Product code LZD·February 2, 1994

    TEFLON PROPLAST INTERPOSITIONAL TMJ

    FDA Adverse Event
    Injury ·VITEK, INC.·Product code LZD·January 28, 1994