BEUDAMED
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    INTERFUSE INVERTEBRAL BODY FUSION DEVICE MODEL 9076

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450800904·

    SYNTHES CERVIFIX/ AXON

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SHANGHAI CHINA STAR CORP POWDERED BLUE NITRILE PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    WAVEWRITER ALPHA PRIME 16

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·November 1, 2024

    CAIMAN DISP. INSTR. NON ARTICUL. D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AP & CO. KG·Product code GEI·March 27, 2015

    CAIMAN DISP.INSTR.ARTICULAT.D:12/240MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·April 6, 2015

    CAIMAN DISP.INSR.ARTICULAT.D:12 / 240MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG& CO. KG·Product code GEI·April 15, 2015

    CAIMAN DISP INSTR ARTICULAT D:12/240MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·April 16, 2014

    MNS UNKNOWN STRATA VALVE/SHUNT

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROSURGERY·Product code JXG·May 1, 2013

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·September 16, 2014

    UNK - IOL

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·April 20, 2011

    Stryker Oasys Midline Occiput Plate-1) Small 2) Medium 3) Large 4) Large Long 5) Mini. Allows for positioning directly on the midline keel of the occiput.

    FDA Enforcement
    Class I ·Terminated·Stryker Spine·August 28, 2013

    CAIMAN DISP. INSTR. ARTICULAT. D.: 12/440MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·July 28, 2014

    145-DEG PE 36MM HUM LINER +0

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWS·December 10, 2024

    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