BEUDAMED
    44 results · 23ms · 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.
    Filters Regulation: Us FDA ×

    Somnera System

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DJO SURGICAL

    FDA UDI
    DJO, LLC·00888912150637·RSP BASEPLATE DRILL LOCKING SCREW GUIDE - REDUC...

    NA

    FDA UDI
    Synthes GmbH·10886982141453·1.3MM CORTEX SCREW SELF-TAPPING 18MM

    Trial Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964083426·Trial Procedure Kit

    Trial Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964083433·Trial Procedure Kit

    VagiVital Aktivgel

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    STCC

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·July 16, 2024

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·August 21, 2023

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·February 23, 2023

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·October 7, 2025

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·July 13, 2023

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·August 20, 2025

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·June 11, 2024

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·March 6, 2023

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·April 20, 2023

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·December 8, 2023

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·January 8, 2025

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·September 24, 2023

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·June 11, 2024