BEUDAMED
    9 results · 49ms · 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 Regulation: Us FDA ×

    RADMAN IMAGE MANAGMENT SYSTEM

    FDA 510(k)
    FDA Class 1 ·Radiology

    Cortera

    FDA UDI
    Xtant Medical Holdings, Inc.·00840311209217·Guidewire, Nitinol, Threaded Tip, 350

    Restore

    FDA UDI
    KEYSTONE DENTAL, INC.·D768R93035048K0·Abutment Screw

    PROCELLERA

    FDA 510(k)
    FDA Unclassified ·Unknown

    EXPRESS MINI GLAUCOMA SHUNT

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    ACRYSOF IQ TORIC

    FDA Adverse Event
    Injury ·ALCON MANUFACTURING, LTD./ HUNTINGTON·Product code HQL·January 22, 2013

    LEAD MODEL 302

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·November 24, 2010

    HEARTMATE II LVAS

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·July 11, 2014

    EMBRYO RPLCMNT CATHETER

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code MQF·September 24, 2019