BEUDAMED
    617 results · 23ms · Sources: EU EUDAMED, US FDA

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    KINOVA

    FDA Adverse Event
    Malfunction ·KINOVA·Product code IQZ·July 26, 2024

    I-LIMB ACCESS

    FDA Adverse Event
    Death ·TOUCH BIONICS LTD.·Product code IQZ·August 31, 2023

    FLEXCELL

    FDA Adverse Event
    Malfunction ·INFINITE BIOMEDICAL TECHNOLOGIES LLC·Product code IQZ·September 24, 2022

    FLEXCELL MINI

    FDA Adverse Event
    Malfunction ·INFINITE BIOMEDICAL TECHNOLOGIES LLC·Product code IQZ·August 25, 2022

    FLEXCELL

    FDA Adverse Event
    Malfunction ·INFINITE BIOMEDICAL TECHNOLOGIES LLC·Product code IQZ·July 8, 2022

    FLEXCELL

    FDA Adverse Event
    Malfunction ·INFINITE BIOMEDICAL TECHNOLOGIES LLC·Product code IQZ·July 8, 2022

    JACO

    FDA Adverse Event
    Injury ·KINOVA·Product code IQZ·August 22, 2022

    FLEXCELL

    FDA Adverse Event
    Malfunction ·INFINITE BIOMEDICAL TECHNOLOGIES LLC·Product code IQZ·July 8, 2022

    SPECTRE GROUP

    FDA Adverse Event
    Malfunction ·GOLDEN PACIFIC ELECTRONICS·Product code IQZ·February 26, 2005

    FLEXCELL

    FDA Adverse Event
    Malfunction ·INFINITE BIOMEDICAL TECHNOLOGY, LLC·Product code IQZ·December 12, 2024

    FLEXCELL

    FDA Adverse Event
    Malfunction ·INFINITE BIOMEDICAL TECHNOLOGIES LLC·Product code IQZ·June 5, 2025

    FLEXCELL

    FDA Adverse Event
    Malfunction ·INFINITE BIOMEDICAL TECHNOLOGIES LLC·Product code IQZ·July 8, 2022

    MYOMOPRO 2X

    FDA Adverse Event
    Injury ·MYOMO, INC.·Product code IQZ·February 19, 2026

    MYOENERGY INTEGRAL

    FDA Adverse Event
    Malfunction ·OTTO BOCK HEALTHCARE PRODUCTS GMBH·Product code IQZ·April 15, 2016

    Spectre brand AC wall adapter to be used with ProControl 2 or ProHand battery powered upper limb prosthesis.

    FDA Recall
    Terminated ·Motion Control, Inc.·Product code IQZ·February 1, 2005

    KINOVA Jaco assistive robot. Model Numbers: PJ 0000 0001, PJ 0000 0012, PJ 0090 0001, PJ 0090 0006, KR MJ2 0001. Jaco replaces the function of the upper limb on one side of the body.

    FDA Recall
    Open, Classified ·Kinova Inc·Product code IQZ·August 22, 2024

    Hand, External Limb Component, Powered

    FDA classification
    FDA Class 1 ·Hand, External Limb Component, Powered

    IMZ

    FDA UDI
    Preat Corporation·00842092115282·IMZ 3.3mm Post Abutment

    IMZ

    FDA UDI
    Preat Corporation·00842092115350·IMZ 4.0mm Post Abutment

    NA

    FDA UDI
    SOUTHERN IMPLANTS (PTY) LTD·06009544027195·Transfer Impression Coping for Int. Hex, Two Pa...