BEUDAMED
    8 results · 20ms · 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 ×

    COBALT-CHROMIUM-MOLYBDENUM (CO-CR-MO) ALLOY FEMORAL HEADS W/CO-NIDIUM SURFACE TREATMENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VSTAAR AdjusteR

    FDA 510(k)
    FDA Unclassified ·Unknown

    SLIDE, LAB-TEK COVERED MICRO

    FDA 510(k)
    FDA Class 1 ·Pathology

    TITANIUM NEXGEN LCCL FEMORAL SZ C-LT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 21, 2018

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 24, 2014

    1.8MM VA LOCKING BUTTRESS PIN WITH T8 STARDRIVE RECESS/18MM

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code HWC·February 14, 2013

    MITROFLOW AORTIC PERICARDIAL HEART VALVE

    FDA Adverse Event
    Other ·SORIN GROUP CANADA INC. MITROFLOW DIVISION·Product code LWR·January 7, 2011

    NEXGEN LEGACY POSTERIOR STABILIZED ARTICULAR SURFACE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·June 16, 2016