BEUDAMED
    2,306 results · 24ms · Sources: EU EUDAMED, US FDA

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    AROX 45 JEP

    FDA Adverse Event
    Malfunction ·BIOTRONIK GMBH AND CO.·Product code DTB·May 6, 2009

    COREVALVE TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·December 20, 2017

    ACCUTRAK DELIVERY CATHETER SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·December 20, 2017

    CA-JR TOFFLEMIRE TYPE RET

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES MANSFIELD·Product code JEP·April 17, 2026

    TOFFELMIRE RETAINER

    FDA Adverse Event
    Malfunction ·SULLIVAN-SCHEIN DENTAL·Product code JEP·April 21, 2005

    AGGA

    FDA Adverse Event
    Injury ·UNKNOWN·Product code JEP·September 27, 2023

    RETAINER

    FDA Adverse Event
    Injury ·RAINTREE ESSEX·Product code JEP·July 24, 2014

    "AGGA", FAGGA, OSSEO-RESTORE APPLIANCE, ARA

    FDA Adverse Event
    Injury ·JOHNS DENTAL LABORATORIES·Product code JEP·March 7, 2023

    ANTERIOR GROWTH GUIDANCE APPLIANCE

    FDA Adverse Event
    Injury ·UNKNOWN·Product code JEP·March 20, 2023

    AGGA

    FDA Adverse Event
    Injury ·ORTHOMATRIXCORP, INC·Product code JEP·March 20, 2023

    AGGA

    FDA Adverse Event
    Injury ·UNKNOWN·Product code JEP·September 27, 2023

    AGGA DENTAL DEVICE

    FDA Adverse Event
    Injury ·UNK·Product code JEP·April 10, 2023

    ANTERIOR GROWTH GUIDANCE APPLIANCE

    FDA Adverse Event
    Injury ·UNK·Product code JEP·April 13, 2023

    UNIVER TOFFLEMIRE TYPE RE

    FDA Adverse Event
    Injury ·INTEGRA YORK, PA INC.·Product code JEP·October 18, 2016

    UNIVER TOFFLEMIRE TYPE RE

    FDA Adverse Event
    Malfunction ·INTEGRA YORK, PA INC.·Product code JEP·August 31, 2016

    ANTERIOR GROWTH GUIDANCE APPLIANCE (AGGA) FAGGA, OSSEO-RESTORATION APPLIANC

    FDA Adverse Event
    Injury ·JOHNS DENTAL LABORATORIES·Product code JEP·April 4, 2023

    MAPES EXPANDER

    FDA Adverse Event
    Injury ·UNKNOWN·Product code JEP·March 16, 2026

    SYCAMORE WOOD WEDGES

    FDA Adverse Event
    Malfunction ·PREMIER DENTAL PRODUCTS COMPANY·Product code JEP·February 18, 2026

    Retainer, Matrix

    FDA classification
    FDA Class 1 ·Retainer, Matrix

    J.P. GILBERT CO.

    FDA registration
    J.P. GILBERT CO.·1 product·🇺🇸 United States