BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    LIGHTWEAR(TM) SYST (LIGHTWEAR HEADLIGHT CLIP/HEADBAND)

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

    LP Low Profile

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746091629·DB BKT LP V-SLOT UL CUSP 018 T=0 A+5 R=0

    OMNI Knee

    FDA UDI
    Omni Life Science, Inc.·00841690101710·Ultra Tibial Insert CS, Size 4 x 18mm

    CLARUS ENDOSCOPIC BALL PROBE

    FDA 510(k)
    FDA Class 1 ·Neurology

    SAFE-PICC CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    V.A.C. THERAPY

    FDA Adverse Event
    Injury ·KCI USA INC.·Product code OMP·June 23, 2014

    SAGITTAL SAW ATTACHMENT

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code HRX·January 30, 2013

    INRATIO2

    FDA Adverse Event
    Other ·ALERE SAN DIEGO, INC.·Product code GJS·December 15, 2010