BEUDAMED
    6 results · 30ms · 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.

    VES-10 INTRAOCULAR SCISSORS DRIVE

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    MENSTRUAL PADS

    FDA 510(k)
    FDA Class 1 ·Obstetrics/Gynecology

    UNIVERSAL SELF-ALIGNING ACETABULAR COM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    12/14 ARTICUL 40MM M SPEC+1.5

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. ¿ REG. # 8010379·Product code LPH·June 10, 2014

    COGNIS

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·October 11, 2010

    2.4/2.7MM VA-LCP FIRST TMT FUSION PLATE/STANDARD

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code HRS·December 10, 2012