BEUDAMED
    8 results · 17ms · 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.

    450/800 DRILL

    FDA 510(k)
    FDA Class 2 ·Neurology

    ERA® Implant Abutment Micro 0°, 5mm Cuff (AX)

    FDA UDI
    STERNGOLD DENTAL LLC·00841549103858·Implant retained overdentures are an establishe...

    2.4MM SYSTEM

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036070915·

    POWEREASE System

    FDA 510(k)
    FDA Class 2 ·Neurology

    MODIFICATION TO ALLOY PRIMER

    FDA 510(k)
    FDA Class 2 ·Dental

    NAVIFLEX? RX DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - SPENCER·Product code FGE·May 15, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 31, 2012

    TOTAL HIP BALL 32MM +11

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code JDI·August 16, 2010