BEUDAMED
    6 results · 19ms · 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 ×

    CustomizedBone Service

    FDA 510(k)
    FDA Class 2 ·Neurology

    PINPOINTE FOOTLASER

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

    LIGHTLAS MULTI-WAVELENGTH MEDICAL LASER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    ALTRX +4 10D 32IDX50OD

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code LPH·October 22, 2014

    LEICA ASP300

    FDA Adverse Event
    Injury ·LEICA BIOSYSTEMS NUSSLOCH GMBH·Product code IEO·June 25, 2013

    CELL-DYN RUBY ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION·Product code GKZ·August 5, 2011