BEUDAMED
    63 results · 22ms · Sources: EU EUDAMED, US FDA

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    AVELLE Negative Pressure Wound Therapy System

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

    BALANCE MICROPLASTY HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304446441·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694034111·Profile Zero Y Plate

    LOCATOR F-Tx

    FDA UDI
    Zest Anchors, LLC·00840481122507·LOCATOR F-Tx Abutment for 2.9mm Platform Conica...

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776187606·Probe with Eye malleable stainless

    LOCATOR R-Tx

    FDA UDI
    Zest Anchors, LLC·00840481122682·LOCATOR R-Tx Attachment System for 2.9mm Platfo...

    Integra® Jarit®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780379614·Integra® Jarit® Probe With Eye, 8"

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694065702·Profile 0 Y Plate Sterile Qty 5

    AAIO-7, AAIO WIRLESS

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    FRONTIER DEVICES NEURO SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    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