BEUDAMED
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    PENTAX Medical Video Duedenoscope ED34-i10T2

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·September 18, 2020

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·November 28, 2020

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·October 23, 2020

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·November 28, 2020

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·August 20, 2021

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·August 18, 2021

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·August 20, 2021

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·August 18, 2021

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·February 25, 2021

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·February 25, 2021

    TWINFIX

    FDA UDI
    Smith & Nephew, Inc.·03596010539304·TWINFIX AB 5.0 MM SUTURE ANCHOR, ...

    Dornier MedTech

    FDA UDI
    Dornier MedTech GmbH·04049958001789·400 Micron Disposable Laser Lightguide, 0.37NA,...

    Dornier MedTech

    FDA UDI
    DORNIER MEDTECH AMERICA, INC.·00810116022427·400 micron core/730 micron OD Luer Lock Diode L...

    Zavation

    FDA UDI
    Zavation LLC·00842166132382·Ti3Z CIF 13mmx15mmx10mm -7 deg

    TiWAVE L Lumbar Cage System

    FDA UDI
    Kalitec Direct LLC·B07323K0107100·Tamp, Rotating

    neoWave LS

    FDA UDI
    XENIX MEDICAL LLC·00818345023796·Angled Tamp

    AQUILION PRIME

    FDA 510(k)
    FDA Class 2 ·Radiology

    SEEDLING ENTERPRISES LLC, COOL TEC MONOPOLAR AND BIPOLAR REUSABLE ELECTRODES

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

    GMK REVISION TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·September 26, 2025