BEUDAMED
    8 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 ×

    MICRO TITANIUM PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    FOR PLAY, SLIP, PREPAIR - PERSONAL LUBRICANTS

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    chromID MRSA

    FDA 510(k)
    FDA Class 2 ·Microbiology

    MENTOR SMOOTH ROUND MODERATE PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·July 31, 2018

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC MILACA, INC.·Product code LWP·February 9, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·January 6, 2011

    VARIAX DR AIMING BLOCK FIXATION PIN

    FDA Adverse Event
    Malfunction ·STRYKER LEIBINGER FREIBURG (MDR)·Product code HRS·July 23, 2014

    Exactech Equinoxe GLENOID, POSTERIOR AUGMENT,PEGGED, CEMENTED, 8o, LEFT, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314-02-22, b) 41, 44, 47, 50 head, Medium, Item Number 314-02-23, c) 44, 47, 50, 53 head, Large, Item Number 314-02-24, d) 44, 47, 50, 53 head, Extra Large, Item Number 314-02-25; Shoulder Arthroplasty

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