BEUDAMED
    12 results · 66ms · 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 ×

    OSSEOTITE

    FDA Adverse Event
    Injury ·BIOMET 3I, LLC·Product code DZE·August 9, 2023

    IMPLANT, ENDOSSEOUS, ROOT-FORM

    FDA Adverse Event
    Malfunction ·BIOMET 3I, LLC·Product code DZE·August 12, 2023

    ENCODE

    FDA Adverse Event
    Injury ·BIOMET 3I, LLC·Product code NHA·August 9, 2023

    DENTAL IMPLANT

    FDA Adverse Event
    Injury ·BIOMET 3I, LLC.·Product code DZE·June 5, 2024

    PANA SPLAY PLUS

    FDA Adverse Event
    Malfunction ·BIOMET 3I LLC·Product code EFB·June 20, 2024

    DENTAL IMPLANT

    FDA Adverse Event
    Malfunction ·BIOMET 3I, LLC·Product code NDP·May 30, 2023

    DENTAL IMPLANT

    FDA Adverse Event
    Malfunction ·BIOMET 3I, LLC·Product code NDP·May 30, 2023

    DENTAL IMPLANT

    FDA Adverse Event
    Malfunction ·BIOMET 3I, LLC·Product code NDP·May 30, 2023

    DENTAL IMPLANT

    FDA Adverse Event
    Injury ·BIOMET 3I, LLC·Product code DZE·April 10, 2025

    ABUTMENT, IMPLANT DENTAL ENDOSSEOUS

    FDA Adverse Event
    Injury ·ZIMVIE / BIOMET 3I, LLC·Product code NHA·July 24, 2024

    DENTAL ABUTMENT

    FDA Adverse Event
    Injury ·ZIMVIE/BIOMET 3I, LLC·Product code NHA·August 1, 2024

    LARGE HEX SCREWDRIVER

    FDA Adverse Event
    Malfunction ·ZIMMER INC. (BIOMET 3I, LLC )·Product code HXX·April 24, 2018