BEUDAMED
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    SHOWER STRETCHER W/WHEELS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Patterson®

    FDA UDI
    PATTERSON DENTAL SUPPLY, INC.·D6620708847592·LATEX PATIENT EXAMINATION GLOVE

    SURGICAL SCALPEL BLADES & DISPOSABLES

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    AMERICAN STERILE MAYO STAND TRAY

    FDA 510(k)

    RIATA ST ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·June 19, 2014

    UNK DEPUY ASR ACETABULAR CUP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·October 22, 2010

    LISTERINE TOOTHBRUSH ULTRA WHITE FIRM

    FDA Adverse Event
    Malfunction ·NI·Product code EFW·December 26, 2012

    Stryker T2 Arthrodesis Nailing System. Manufacturer: Stryker Trauma GmbH, Professor-Kuntscher-Str. 1-5, 24232 Schonkirchen Germany. Distributed in the USA by Stryker Orthopaedics, 325 Corporate Drive, Mahwah, NJ 07430. The T2 Arthrodesis Nail is intended for the treatment of Knee Arthrodesis. The design of the T2 Arthrodesis Nail features a unique curvature which incorporates both femur ante curvature and knee valgus bend. Indications: Aseptic failed total knee arthro-plasty with or without bone loss; Failed external fixation, non unions and malunions; Periarticular fractures where repair is not possible; Pathologic fractures and tumor resections; Pseudoarthrosis and correct osteotomy; Ipsilateral femur fractures; and Open and closed femoral fractures.

    FDA Enforcement
    Class II ·Terminated·Stryker Howmedica Osteonics Corp.·July 25, 2012