BEUDAMED
    7 results · 21ms · 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 ×

    LARYNGEAL STENT

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    MODIFICATION TO EN-BLOC BIOPSY SYSTEM

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

    EMERGE MEDICAL IM NAIL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PFC SIGMA CRVD INSERT SZ3 8MM

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JWH·May 1, 2019

    M2A-MAGNUM MOD HEAD SZ 46MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·May 30, 2014

    PRIMUS HI

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SOLUTIONS USA, INC.·Product code IYE·October 23, 2012

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·September 13, 2010