BEUDAMED
    46 results · 38ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    HENRY SCHEIN

    FDA Adverse Event
    Injury ·HANDPIECE HEADQUARTERS·Product code EFB·March 21, 2024

    MIDWEST

    FDA Adverse Event
    Injury ·HANDPIECE HEADQUARTERS·Product code EFB·March 21, 2023

    W&H

    FDA Adverse Event
    Injury ·HANDPIECE HEADQUARTERS·Product code EFB·April 17, 2025

    MAXIMA PRO 45 N/O FIXED END

    FDA Adverse Event
    Injury ·HANDPIECE HEADQUARTERS·Product code EFB·October 1, 2022

    DARBY

    FDA Adverse Event
    Injury ·HANDPIECE HEADQUARTERS·Product code EFB·December 28, 2023

    MAXIMA PRO 45 N/O FIXED END

    FDA Adverse Event
    Injury ·HANDPIECE HEADQUARTERS·Product code EFB·September 7, 2022

    HENRY SCHEIN PRECISION-TORQUE

    FDA Adverse Event
    Malfunction ·HANDPIECE HEADQUARTERS INC.·Product code EFB·May 29, 2019

    IMPACT AIR 45

    FDA Adverse Event
    PALISADES DENTAL, LLC·Product code EFB·November 9, 2015

    BA INTERNATIONAL 1:5 HANDPIECE

    FDA Adverse Event
    Injury ·B.A. INTERNATIONAL LTD.·Product code EGS·November 12, 2020

    RENEW XR HANDPIECE, 34CM

    FDA Adverse Event
    Malfunction ·MICROLINE SURGICAL INC·Product code GEI·May 20, 2024

    BA INTERNATIONAL 1:5 HANDPIECE

    FDA Adverse Event
    Injury ·B.A. INTERNATIONAL LTD.·Product code EGS·November 12, 2020

    NSK X95L

    FDA Adverse Event
    NAKANISHI INC.·Product code EGS·July 21, 2015

    AHP-77C 1:2 ANGLED HANDPIECE

    FDA Adverse Event
    Injury ·NSK NAKANISHI·Product code EFB·June 23, 2010

    AQUABEAM ROBOTIC SYSTEM

    FDA Adverse Event
    Malfunction ·PROCEPT BIOROBOTICS CORPORATION·Product code PZP·June 23, 2023

    AQUABEAM ROBOTIC SYSTEM

    FDA Adverse Event
    Malfunction ·PROCEPT BIOROBOTICS CORPORATION·Product code PZP·July 10, 2023

    PROFOUND SYSTEM (FORMERLY KNOWN AS MIRATONE SYSTEM)

    FDA Adverse Event
    Injury ·SYNERON MEDICAL LTD.·Product code GEI·August 19, 2016

    GENTLEMINI LUX 4500 BR

    FDA Adverse Event
    Injury ·KAVO DENTAL GMBH·Product code EFB·October 10, 2012

    KAVO

    FDA Adverse Event
    Injury ·KAVO DENTAL·Product code EFB·July 13, 2010

    CUSA EXCEL 36KHZ STRAIGHT HANDPIECE

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES(IRELAND)·Product code LFL·July 15, 2020

    CUSA EXCEL 36KHZ STRAIGHT HANDPIECE

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES(IRELAND)·Product code LFL·July 15, 2020