BEUDAMED
    8 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.

    MICROSURGICAL KERATOME

    FDA 510(k)
    FDA Class 1 ·Neurology

    FORZA

    FDA UDI
    Orthofix US LLC·18257200077229·9W X 27L X 0° X 16H STRAIGHT TRIAL

    Durasphere ® EXP

    FDA UDI
    Carbon Medical Technologies, Inc.·00858015005011·Injectable Bulking Agent

    SpaceFlex Knee

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    COLLAGEN DENTAL MEMBRANE IV

    FDA 510(k)
    FDA Class 2 ·Dental

    RESTORE ADVANCED RECHARGEABLE

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·October 22, 2010

    FORTIFY VR, DF-4 CONNECTOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL INC., CRMD·Product code LWS·January 13, 2014

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·December 28, 2012