BEUDAMED
    9 results · 18ms · 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.

    DISPOSABLE SCREW TYPE PROPHY BRUSH

    FDA 510(k)
    FDA Class 1 ·Dental

    Trial Tibial Augment

    FDA UDI
    ADLER ORTHO SPA·08056269043618·TRIAL PANTHEON TIBIAL AUGMENT LM/RL SIZE 7 H5

    Master Series

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746135668·DB BKT MASTER UR CUSP 022 T=0 A+8 R=0

    ZAVATION

    FDA UDI
    Zavation LLC·00842166151093·WHITNEY 12mmx14mm , 5deg , 07mm

    CAVERMAP SURGICAL AID

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    MODIFICATION TO LDR SPINE ROI INTERBODY FUSION SYSTEM; ROI-A IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    IMPLANTIUM

    FDA Adverse Event
    Injury ·DENTIUM USA·Product code DZE·June 27, 2014

    ASR ACETABULAR CUPS 50

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·January 7, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·November 16, 2010