BEUDAMED
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    S&C-SELF ETCH PR-BOND

    FDA 510(k)
    FDA Class 2 ·Dental

    Bard® LeFort Metal Sound

    FDA UDI
    C. R. Bard, Inc.·00801741032455·Bard LeFort Metal Sound, Threaded Tip, Stainles...

    MILLENNIUM

    FDA UDI
    Avalign Technologies, Inc.·00190776315771·Probe

    Entuit Thrive LP

    FDA UDI
    XERIDIEM MEDICAL DEVICES, INC.·00827002356474·

    KENDALL, SEQUENTIAL COMPRESSION DEVICE; HUNTLEIGH, FLOWTRON; VENAFLOW; ACUFEX; ALPS; SHEEPSKIN

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ADVENT IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 2, 2013

    VITALITY DS VR

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC·Product code LWS·May 8, 2008

    DYNASTY(R) COCR LINER

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code JDL·April 6, 2011

    Stryker MA204 Bed Model (FL25E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of the bed.The devices listed above also include movable and latchable side rails which can be lowered or raised to help prevent patient fall and subsequent injury. The Beds include an optional Scale (Models: FL20E, FL25E, FL28C, FL28EX) as well as an optional Bed Exit (1 Zone) or Chaperone

    FDA Enforcement
    Class II ·Terminated·Stryker Medical Division of Stryker Corporation·July 4, 2012