BEUDAMED
    6 results · 21ms · 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 ×

    HELIOMOLAR(R) DENTAL RESTORATIVE

    FDA 510(k)
    FDA Class 2 ·Dental

    OXYMIZER-PENDANT

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    INSTA-GLAZE

    FDA 510(k)
    FDA Class 1 ·Dental

    BECKER TEARDROP 3MM 26CM LG

    FDA Adverse Event
    MENTOR WORLDWIDE LLC·Product code MUU·June 11, 2014

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·October 22, 2010

    EZ STEER ¿ THERMOCOOL® BI-DIRECTIONAL CATHETER

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code OAD·December 23, 2012