BEUDAMED
    9 results · 23ms · 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 ×

    NeuroBlate System

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

    BD BBL™ Taxo™ Differentiation Discs for Dextrose

    FDA UDI
    BECTON, DICKINSON AND COMPANY·00382902310617·BD BBL™ Taxo™ Differentiation Discs for Dextrose

    Intrigue

    FDA UDI
    LANCER ORTHODONTICS, INC.·00817573021031·INTRG WHISP ROTH 1BIC HK-17T 0A 018 LR

    Symmetry Surgical

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482001462·Symmetry® Curette, Spinal, Straight, Size 000, ...

    NEXGEN POROUS, UNCEMENTED FEMORAL AND TIBIAL BASEPLATE COMPONENTS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RESTORE BUNION CORRECTION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    S-ROM STEM BODY TRIAL 16

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code LXH·October 29, 2008

    HEARTSTART MRX-EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE - ANDOVER·Product code MKJ·July 20, 2011

    PLUM XLD 110V L.A.

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·July 12, 2013