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.

    LED STIMULATOR LS-05

    FDA 510(k)
    FDA Class 2 ·Neurology

    PHADEBAS & PHADEZYM RAST ALLERGEN DISCS

    FDA 510(k)
    FDA Class 2 ·Immunology

    PRISMA-FINE

    FDA 510(k)
    FDA Class 2 ·Dental

    CONTINUOUS WAVE III ARTHROSCOPY PUMP

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HRX·May 28, 2014

    NC TREK CORONARY DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code LOX·November 15, 2012

    CENTRICITY WEB-DX

    FDA Adverse Event
    Malfunction ·GE HEALTHCARE·Product code LLZ·September 10, 2010

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·January 22, 2020

    Exactech Equinoxe GLENOID,KEELED, CEMENTED, mates with 47, 50, 53 head, beta curvature, Sizes: a) Small, Item Number 314-01-12, b) Medium, Item Number 314-01-13, c) Large, Item Number 314-01-14, Shoulder Arthroplasty

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·April 10, 2024