BEUDAMED
    6 results · 22ms · 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.

    I-SPOUSE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    ASCENT PIT & FISSURE SEALANT

    FDA 510(k)
    FDA Class 2 ·Dental

    'cottony' II TAPE, PLEDGETS

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ATTAIN

    FDA Adverse Event
    Injury ·MPRI·Product code LWP·February 9, 2013

    M2A MAGNUM PF CUP 50MM O.D. X 44 MM I.D.

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·January 7, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 23, 2014