BEUDAMED
    353 results · 41ms · Sources: EU EUDAMED, US FDA

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    HIGH PULL HEADGEAR

    FDA Adverse Event
    Injury ·ORMCO CORPORATION·Product code DZB·April 11, 2014

    ORTHODONTIC FACEMASK

    FDA Adverse Event
    Malfunction ·Product code DZB·June 22, 2021

    FACEBOW

    FDA Adverse Event
    Injury ·ORMCO CORPORATION·Product code DZB·November 6, 2017

    A.D. PROTRACTION FASKMASK

    FDA Adverse Event
    Injury ·ORMCO CORPORATION·Product code DZB·December 17, 2018

    PROTRACTION FACEMASK

    FDA Adverse Event
    Injury ·GAC INTERNATIONAL·Product code DZB·February 26, 2013

    ADAPTABLE CLASS III MASK

    FDA Adverse Event
    Injury ·GREAT LAKES ORTHODONTICS, LTD.·Product code DZB·July 31, 2011

    ADAPTABLE CLASS III MASK

    FDA Adverse Event
    Injury ·GREAT LAKES ORTHODONTICS LTD·Product code DZB·August 30, 2011

    NONE

    FDA Adverse Event
    Injury ·"A" COMPANY ORTHODONTICS·Product code DZB·July 23, 1997

    FACE BOW

    FDA Adverse Event
    Injury ·AMERICAN ORTHODONTICS·Product code DZB·March 14, 2007

    HIGH-PULL HEADCAP

    FDA Adverse Event
    Injury ·HOOD-GEAR PACIFIC, INC.·Product code DZB·April 25, 1995

    FACE BOW

    FDA Adverse Event
    AMERICAN ORTHODONTICS·Product code DZB·November 8, 2005

    UNK

    FDA Adverse Event
    Injury ·UNK·Product code DZB·August 26, 2002

    FRICTION - STOP ADJUSTABLE FACEBOW

    FDA Adverse Event
    Malfunction ·3M UNITEK·Product code DZB·October 31, 2001

    DENTAL IMPLANT

    FDA Adverse Event
    Malfunction ·UNK·Product code DZB·May 4, 2026

    ORMCO C-TYPE RELEASE MODULES

    FDA Adverse Event
    Malfunction ·ORMCO CORP.·Product code DZB·March 17, 1998

    ORMCO C-TYPE RELEASE MODULES

    FDA Adverse Event
    Malfunction ·ORMCO CORP.·Product code DZB·March 17, 1998

    ORMCO C-TYPE RELEASE MODULES

    FDA Adverse Event
    Malfunction ·ORMCO CORP.·Product code DZB·March 17, 1998

    Headgear, Extraoral, Orthodontic

    FDA classification
    FDA Class 2 ·Headgear, Extraoral, Orthodontic

    Insulated Needle

    FDA UDI
    Cynosure, LLC·00841494104054·NEEDLE .007 FINE WIRE, PURPLE, 1/16" SHT

    LUCIRA CHECK-IT COVID-19 TEST

    FDA Adverse Event
    Malfunction ·PFIZER, INC.·Product code QJR·July 13, 2023