BEUDAMED
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    P.F.C. HIP SYSTEM NON-POROUS FEMORAL COMPONENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Ear Holder Disposable Cover

    FDA UDI
    PaloDEx Group Oy·06430035873517·

    Upper ROC Pack for Herbst UL6

    FDA UDI
    SPECIALTY APPLIANCES, LLC·D8199006380·

    TCP

    FDA UDI
    WRIGHT MEDICAL TECHNOLOGY, INC.·00840420118660·

    RESPONDER 3000

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    GENADYNE A4-XLR8 WOUND VACUUM SYSTEM

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

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 27, 2014

    MAXCEM ELITE

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EMA·January 7, 2013

    TOTALCARE BARIATRIC

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·November 9, 2010

    ENF-GP2 Rhino-Laryngo Fiberscope - Product Usage: is indicated for use within the nasal and nasopharyngeal lumen.

    FDA Enforcement
    Class II ·Terminated·Olympus Corporation of the Americas·June 17, 2020