BEUDAMED
    134 results · 50ms · Sources: EU EUDAMED, US FDA

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    ACTIFLO

    FDA Adverse Event
    Injury ·ROBLING MEDICAL, INC.·Product code KNT·March 10, 2014

    FIBULINK SYNDESMOSIS REPAIR KIT/SS

    FDA Adverse Event
    Malfunction ·AKROS MEDICAL, INC·Product code HTN·August 5, 2021

    FIBULINK SYNDESMOSIS REPAIR KIT/SS

    FDA Adverse Event
    Malfunction ·AKROS MEDICAL, INC·Product code HTN·April 1, 2021

    FIBULINK SYNDESMOSIS REPAIR KIT/SS

    FDA Adverse Event
    Injury ·WRIGHTS LANE : SYNTHES USA PRODUCTS LLC·Product code HTN·August 26, 2021

    FIBULINK SYNDESMOSIS REPAIR KIT/SS

    FDA Adverse Event
    Injury ·AKROS MEDICAL, INC·Product code HTN·June 22, 2021

    FIBULINK SYNDESMOSIS REPAIR KIT TI

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HTN·September 16, 2024

    FIBULINK® SYNDESMOSIS REPAIR KIT/ TI

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HTN·November 19, 2025

    FIBULINK® SYNDESMOSIS REPAIR KIT/SS

    FDA Adverse Event
    Malfunction ·AKROS MEDICAL, INC·Product code HTN·November 18, 2021

    FIBULINK SYNDESMOSIS REPAIR KIT/TI

    FDA Adverse Event
    Malfunction ·AKROS MEDICAL, INC·Product code HTN·July 20, 2021

    FIBULINK SYNDESMOSIS REPAIR KIT/SS

    FDA Adverse Event
    Malfunction ·AKROS MEDICAL, INC·Product code HTN·July 1, 2021

    FIBULINK® SYNDESMOSIS REPAIR KIT/ TI

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HTN·August 11, 2025

    FIBULINK® SYNDESMOSIS REPAIR KIT/SS

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HTN·April 25, 2023

    FIBULINK® SYNDESMOSIS REPAIR KIT/ TI

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HTN·March 9, 2026

    FIBULINK® SYNDESMOSIS REPAIR KIT/SS

    FDA Adverse Event
    Malfunction ·MONUMENT DEPUY SYNTHES PRODUCTS INC·Product code HTN·March 7, 2022

    FIBULINK® SYNDESMOSIS REPAIR KIT/SS

    FDA Adverse Event
    Malfunction ·MONUMENT DEPUY SYNTHES PRODUCTS INC·Product code HTN·January 6, 2022

    ULTRACISION HARMONIC ACE (EXACT CODE UNKNOWN)

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·January 6, 2020

    Atec Insignia Anterior Cervical Plate System, REF 136-0120, Insignia, ACP, 1-Level, 20 mm, Rx Only, Non-Sterile, UDI: (01)00190376268460

    FDA Recall
    Terminated ·Alphatec Spine, Inc. 1950 Camino Vida Roble·Product code KWQ·April 26, 2021

    Atec Insignia Anterior Cervical Plate System, REF 136-0468 Insignia, ACP, 4-Level, 68 mm, Rx Only, Non-Sterile, UDI: (01)00190376268675

    FDA Recall
    Terminated ·Alphatec Spine, Inc. 1950 Camino Vida Roble·Product code KWQ·April 26, 2021

    Atec Insignia Anterior Cervical Plate System, REF 136-0122, Insignia, ACP, 1-Level, 22 mm, Rx Only, Non-Sterile, UDI: (01)00190376268484

    FDA Recall
    Terminated ·Alphatec Spine, Inc. 1950 Camino Vida Roble·Product code KWQ·April 26, 2021

    Atec Insignia Anterior Cervical Plate System, REF 136-0362 Insignia, ACP, 3-Level, 62 mm, Rx Only, Non-Sterile, UDI: (01)00190376268620

    FDA Recall
    Terminated ·Alphatec Spine, Inc. 1950 Camino Vida Roble·Product code KWQ·April 26, 2021