BEUDAMED
    55 results · 25ms · Sources: EU EUDAMED, US FDA

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    BIO-C REPAIR

    FDA 510(k)
    FDA Class 2 ·Dental

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361014867·Screw Assy REset Cannula 5.0X30mm Gen 3

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361014874·Screw Assy REset Cannula 5.0X35mm Gen 3

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361014904·Screw Assy REset Cannula 5.0X50mm Gen 3

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361014881·Screw Assy REset Cannula 5.0X40mm Gen 3

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361014850·Screw Assy REset Cannula 5.0X25mm Gen 3

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361014898·Screw Assy REset Cannula 5.0X45mm Gen 3

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361014843·Screw Assy REset Cannula 5.0X20mm Gen 3

    AMS ELEVATE WITH INTEPRO LITE PROLAPSE REPAIR SYSTEM, AMS ELEVATE WITH INTEXEN LP PROLAPSE REPAIR SYSTEM

    FDA 510(k)
    FDA Class 3 ·Obstetrics/Gynecology

    SLEEP APP

    FDA 510(k)
    FDA Class 2 ·Dental

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·February 7, 2022

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·October 12, 2022

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·November 17, 2022

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·December 1, 2022

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·March 22, 2023

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·June 13, 2024

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·March 27, 2024

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·January 5, 2023

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·February 5, 2023

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·January 26, 2023