BEUDAMED
    6 results · 42ms · 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.

    GORE-TEX REGENERATIVE MATERIAL TITANIUM REINFORCED CONFIGURATIONS

    FDA 510(k)
    FDA Class 2 ·Dental

    HOTWIRE RF GUIDEWIRE (901XXX); HOTWIRE RF GUIDEWIRE (902XXX)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    KODAK MODELS 2100 AND 2200

    FDA 510(k)
    FDA Class 2 ·Dental

    DHS/DCS-IMPACT F/ONE-STEP INSERT-TECHN F

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code GFA·February 14, 2013

    GRANUFLO

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·July 15, 2014

    UNKNOWN

    FDA Adverse Event
    Other ·ENCORE MEDICAL, L.P.·Product code N/A·January 7, 2011