BEUDAMED
    8 results · 39ms · 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 FDA Adverse Event ×

    SILICONE FINGER IMPLANT - SIZE 4

    FDA Adverse Event
    Malfunction ·OSTEOTEC LIMITED·Product code KYJ·December 5, 2025

    OSTEOTEC

    FDA Adverse Event
    Malfunction ·OSTEOTEC LIMITED·Product code KYJ·December 23, 2025

    OSTEOTEC

    FDA Adverse Event
    Malfunction ·OSTEOTEC LIMITED·Product code KYJ·December 23, 2025

    OSTEOTEC

    FDA Adverse Event
    Malfunction ·OSTEOTEC LIMITED·Product code KYJ·December 23, 2025

    OSTEOTEC

    FDA Adverse Event
    Malfunction ·OSTEOTEC LIMITED·Product code KYJ·April 30, 2026

    20 SILICONE PIP IMPLANT (STERILE PACKED)

    FDA Adverse Event
    Injury ·ENCORE MEDICAL L.P·Product code KYJ·September 11, 2023

    MAGNIFUSE (GRAFTON II EDEM)

    FDA Adverse Event
    Injury ·OSTEOTECH, INC.·Product code MQV·February 8, 2012

    GRAFTON

    FDA Adverse Event
    Injury ·OSTEOTECH·Product code MBP·January 21, 2015