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    SUMMIT SWIVEL COLLIMATOR

    FDA Adverse Event
    Malfunction ·SUMMIT INDUSTRIES, INC.·Product code IZX·June 26, 2007

    SUMMIT SWIVEL COLLIMATOR

    FDA Adverse Event
    Malfunction ·SUMMIT INDUSTRIES, LLC·Product code IZX·July 17, 2014

    PROGENCY, INC

    FDA Adverse Event
    Malfunction ·PROGENY, INC.·Product code IZX·April 23, 1998

    NM MILLENNIUM MPR COLLIMATOR

    FDA Adverse Event
    Injury ·GE MEDICAL SYSTEMS, F.I. HAIFA·Product code IZX·December 30, 2004

    EUREKA LINEAR IIIP

    FDA Adverse Event
    Other ·PROGENY, INC.·Product code IZX·May 21, 1998

    R-30H , Diagnostic X-Ray Beam-Limiting Device. In combination with any of below X-ray tubes 0.6/1.2P364DK-85, 0.6/1.2P324DK-125, 0.6/1.2P324DK-85, 0.6/1.2P38DE-85 Device Model # R-30H. Subsequent Product Code: IZX Product Usage: The device is the beam-limiting device for X-ray Radiography.

    FDA Enforcement
    Class II ·Terminated·Shimadzu Medical Systems·November 14, 2012

    R-30H , Diagnostic X-Ray Beam-Limiting Device. In combination with any of below X-ray tubes 0.6/1.2P364DK-85, 0.6/1.2P324DK-125, 0.6/1.2P324DK-85, 0.6/1.2P38DE-85 Device Model # R-30H. Subsequent Product Code: IZX Product Usage: The device is the beam-limiting device for X-ray Radiography.

    FDA Recall
    Terminated ·Shimadzu Medical Systems·Product code IZW·October 28, 2011

    R-20J , Diagnostic X-Ray Beam-Limiting Device. In combination with any of below X-Ray tubes: 06/1.2P364DK-85, 0.6/1.2P324DK-125, 06/1.2P324DK-85, 0.6/1.2P38DE-85. Product Usage: The device is the beam-limiting device for X-ray Radiography.

    FDA Recall
    Terminated ·Shimadzu Medical Systems·Product code IZX·October 28, 2011

    LX125V Swivel Collimator, Model E600; Manual Radiographic Collimator; Summit Industries, Inc., Chicago, Illinois

    FDA Recall
    Terminated ·Summit Industries Inc.·Product code IZX·August 10, 2007

    PCS125 Swivel Collimator, Model F100; Manual Radiographic Collimator; Summit Industries, Inc., Chicago, Illinois

    FDA Recall
    Terminated ·Summit Industries Inc.·Product code IZX·August 10, 2007

    LX125 Swivel Collimator, Model D800; Manual Radiographic Collimator; Summit Industries, Inc., Chicago, Illinois

    FDA Recall
    Terminated ·Summit Industries Inc.·Product code IZX·August 10, 2007

    Collimator, Manual, Radiographic

    FDA classification
    FDA Class 2 ·Collimator, Manual, Radiographic

    IOX CO. LTD.

    FDA registration
    IOX CO. LTD.·3 products·🇯🇵 Japan

    IZI MEDICAL PRODUCTS LLC

    FDA registration
    IZI MEDICAL PRODUCTS LLC·16 products·🇺🇸 United States

    TAIZHOU ZIXING GLASSES CO., LTD.

    FDA registration
    TAIZHOU ZIXING GLASSES CO., LTD.·4 products·🇨🇳 China

    Taper-Lock™

    FDA UDI
    ZimVie US Corp LLC·00889024015531·

    Invacare® AVIVA FX Power Wheelchair

    FDA UDI
    INVACARE CORPORATION·00841447111658·Invacare® AVIVA FX Power Wheelchair

    Invacare® AVIVA FX Power Wheelchair

    FDA UDI
    INVACARE CORPORATION·00841447111627·Invacare® AVIVA FX Power Wheelchair

    Invacare® AVIVA FX Power Wheelchair

    FDA UDI
    INVACARE CORPORATION·00841447111634·Invacare® AVIVA FX Power Wheelchair

    Invacare® AVIVA FX Power Wheelchair

    FDA UDI
    INVACARE CORPORATION·00841447111641·Invacare® AVIVA FX Power Wheelchair