BEUDAMED
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    ARIETTA 750

    FDA 510(k)
    FDA Class 2 ·Radiology

    Novo Surgical

    FDA UDI
    NOVO SURGICAL, INC.·00842331122057·Titanium Rhoton Bipolar Bayonet Forceps, round ...

    SYNTHES MATRIXMANDIBLE SUBCONDYLAR PLATES

    FDA 510(k)
    FDA Class 2 ·Dental

    SAFE'N'SOUND PASSIVE DELIVERY SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ONE TOUCH ULTRA

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·October 28, 2002

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 26, 2013

    HAKIM PROGRAMMABLE VALVE, RT ANGLE

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC. MEDOS S.A.·Product code JXG·July 29, 2011

    OBTRYX MESH SLING SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FTL·September 25, 2008

    COSGROVE-EDWARDS ANNULOPLASTY SYSTEM WITH DURAFLO TREATMENT

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code KRH·October 12, 2009

    ONE TOUCH ULTRA2 METER

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code NBW·October 15, 2009