BEUDAMED
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    OMNILUX CLEAR-U

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

    SchureMed

    FDA UDI
    SCHUERCH CORPORATION·00810057370953·GETTINGE / SHAMPANE 1400 1500 1900 SOFTCARE PLU...

    Specials

    FDA UDI
    Seaspine Orthopedics Corporation·10889981291204·Trial Rasp, 14 x 13 x 7mm, 7° Lordosis

    FERRIS POLYMEM SILVER WOUND DRESSING

    FDA 510(k)
    FDA Unclassified ·Unknown

    CONTINUUM KNEE SYSTEM-PS FEMORAL COMPONENTS- POROUS, MODEL XX-YYY-ZZZZZ

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNKNOWN_NEUROVASCULAR_PRODUCT

    FDA Adverse Event
    Injury ·CONCENTRIC MEDICAL·Product code NRY·December 14, 2012

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·April 26, 2013

    RESTORE ULTRA

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·April 21, 2011

    WINGSPAN STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC, NEUROVASCULAR DIV.·Product code NJE·July 22, 2008

    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