BEUDAMED
    6 results · 19ms · 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 ×

    KLS Martin LSS Plating System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODEL 3000 AXYALOOP BIO-ABSORBABLE BONE ANCHOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CRITICAL CARE ASSESSMENT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code LWP·June 7, 2013

    PINNACLE PELVIC FLOOR REPAIR KITS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·July 7, 2011

    LASIK SURGERY

    FDA Adverse Event
    Injury ·Product code LZS·September 7, 2008