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    Cortigent, INC.

    FDA registration
    Cortigent, INC.·1 product·🇺🇸 United States

    Argus II Video Processing Unit (VPU)

    FDA UDI
    CORTIGENT, INC.·00850052743000·The VPU is used to process the images from the ...

    Argus II Glasses - Right Eye - Dark Lenses

    FDA UDI
    CORTIGENT, INC.·00850052743109·The Argus II Glasses provide a convenient and d...

    Argus II Operating Room Coil

    FDA UDI
    CORTIGENT, INC.·00850052743161·

    Argus II Glasses, Left Eye, Clear Lenses

    FDA UDI
    CORTIGENT, INC.·00850052743130·The Argus II Glasses provide a convenient and d...

    Argus II Glasses, Left Eye, Dark Lenses

    FDA UDI
    CORTIGENT, INC.·00850052743123·The Argus II Glasses provide a convenient and d...

    Argus II Glasses, Right Eye, Clear Lenses

    FDA UDI
    CORTIGENT, INC.·00850052743116·The Argus II Glasses provide a convenient and d...

    Argus II Communication Adapter (CA)

    FDA UDI
    CORTIGENT, INC.·00850052743055·A device which provides data communication and ...

    Cascade IOMAX Cortical Module, REF: 190296-200

    FDA Recall
    Open, Classified ·Cadwell Industries Inc·Product code GWF·May 17, 2024

    Cascade IOMAX Cortical Module, REF: 190296-200

    FDA Recall
    Open, Classified ·Cadwell Industries Inc·Product code GWF·April 23, 2024

    DePuy Mitek LATARJET EXPERIENCE Extraction Driver Product Code: 288216 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft

    FDA Recall
    Terminated ·DePuy Mitek, Inc., a Johnson & Johnson Co.·Product code HWC·May 12, 2017

    DePuy Mitek LATARJET EXPERIENCE-Combo Screw Driver Product Code: 288211 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft

    FDA Recall
    Terminated ·DePuy Mitek, Inc., a Johnson & Johnson Co.·Product code HWC·May 12, 2017

    DePuy Mitek LATARJET EXPERIENCE Coracoid Drill Product Code: 288201 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft

    FDA Recall
    Terminated ·DePuy Mitek, Inc., a Johnson & Johnson Co.·Product code HWC·May 12, 2017

    DePuy Mitek LATARJET EXPERIENCE Top Hat Tap Product Code: 288203 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft

    FDA Recall
    Terminated ·DePuy Mitek, Inc., a Johnson & Johnson Co.·Product code HWC·May 12, 2017

    DePuy Mitek LATARJET EXPERIENCE Coracoid Top Hat Drill Product Code: 288202 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft

    FDA Recall
    Terminated ·DePuy Mitek, Inc., a Johnson & Johnson Co.·Product code HWC·May 12, 2017