BEUDAMED
    7 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 ×

    LipiFlow Thermal Pulsation System

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    LASER HAIR GROWTH CAP

    FDA Adverse Event
    Injury ·UNKNOWN·Product code OAP·February 26, 2025

    F.A.S.T. SYSTEM SED AND CXD

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BLUE POWDERFREE NITRILE EXAMINATION GLOVE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 27, 2013

    DEPUY ORTHO

    FDA Adverse Event
    Injury ·DEPUY ORTHO/JOHNSON & JOHNSON·Product code LPH·August 1, 2011

    AGILTRAC

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR DEVICES·Product code LIT·September 29, 2008