BEUDAMED
    6 results · 21ms · 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 ×

    AIM TIBIAL NAIL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LightWalker Laser System Family

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    LORENZ LACTOSORB VOCAL MEDIALIZATION IMPLANT

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    PERFIX PLUG

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·June 26, 2014

    TELIGEN

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·January 11, 2013

    NOVOFINE 8MM (30G) (NEEDLE) NA

    FDA Adverse Event
    NOVO NORDISK A/S, MEDICAL SYSTEMS·Product code FMF·November 24, 2010