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    PACE SURGICAL

    FDA registration
    PACE SURGICAL·10 products·🇺🇸 United States

    Ultra Compression Screw System

    FDA UDI
    Pace Surgical, Inc.·00810211040234·Headed Screw Partially Threaded Short 3.0mm,32m...

    Ultra Compression Screw System

    FDA UDI
    Pace Surgical, Inc.·00810211040845·Headed Screw, Partially Threaded, Short, Diamet...

    Headed Screw Partially Threaded Short 3.0mm,30mm Length

    FDA UDI
    Pace Surgical, Inc.·00810211040227·Headed Screw Partially Threaded Short 3.0mm,30m...

    Ultra Compression Screw System

    FDA UDI
    Pace Surgical, Inc.·00810211040814·Headed Screw, Partially Threaded, Short, 5.5mm,...

    Ultra Compression Screw System

    FDA UDI
    Pace Surgical, Inc.·00810211040821·Headed Screw, Partially Threaded, Short, 6.5mm,...

    Ultra Compression Screw System

    FDA UDI
    Pace Surgical, Inc.·00810211040852·Headed Screw, Partially Threaded, Short, 6.5mm,...

    Ultra Compression Screw System

    FDA UDI
    Pace Surgical, Inc.·00810211040838·Headed Screw, Partially Threaded, Short, 6.5mm,...

    DETECT SURGICAL PACING AND MAPPING TOOL

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·October 9, 2017

    CARDIOBLATE MAPS SURGICAL MAPPING, ABLATION, PACING , AND SENSING DEVICE

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

    INGEVITY

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code LWP·October 10, 2017

    CARDIOBLATE MAPS SURGICAL MAPPING, ABLATION, PACING AND SENSING DEVICE, MODEL 49205

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

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code LWS·September 18, 2024

    INGEVITY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code NVN·January 30, 2026

    INGEVITY?+

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NVN·March 28, 2025

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code LWS·August 26, 2022

    FINELINE II EZ STEROX

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DTB·March 4, 2022

    FINELINE II EZ STEROX

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DTB·October 25, 2024

    ACUITY X4 STRAIGHT

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code LWP·February 15, 2023