BEUDAMED
    10 results · 72ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    HOYA Corporation PENTAX Lifecare Division

    FDA registration
    HOYA Corporation PENTAX Lifecare Division·31 products·🇯🇵 Japan

    HOYA Corporation PENTAX Lifecare Division

    FDA registration
    HOYA Corporation PENTAX Lifecare Division·29 products·🇯🇵 Japan

    PENTAX Europe GmbH

    Authorized representative
    🇩🇪 Germany·4 Manufacturers·142 Devices

    PENTAX MEDICAL VIDEO PROCESSOR EPK-I5010

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX DIVISION·Product code PEA·October 1, 2025

    PENTAX VIDEO GASTROSCOPE

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX DIVISION·Product code FDS·May 24, 2023

    HITACHI

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX DIVISION·Product code IYN·October 7, 2024

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION, PENTAX DIVISION·Product code FDT·February 21, 2018

    PENTAX DUODENOSCOPE

    FDA Adverse Event
    Injury ·PENTAX/ HOYA CORPORATION PENTAX LIFECARE DIVISION·Product code FDT·April 14, 2025

    PENTAX ENDOSCOPY ULTRASOUND

    FDA Adverse Event
    Other ·HOYA CORPORATION PENTAX LIFECARE DIVISION·Product code ODG·July 10, 2024

    PENTAX ENDOSCOPE EG 2990I

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX LIFECARE DIVISION·Product code FDS·August 14, 2024