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 ×

    Disposable Endoscope Valves Kit

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Diamond Digital Sleep Orthotic (DDSO)

    FDA 510(k)
    FDA Class 2 ·Dental

    AIRCAST VENAFLOW ELITE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    S-ROM HEAD FEMORAL COCR 32+3

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code JDG·November 5, 2008

    PRIME ZOOM STRETCHER, 26" LITTER

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code INK·July 13, 2011

    INTERSTIM

    FDA Adverse Event
    Malfunction ·NEURO - VILLALBA·Product code EZW·July 12, 2013

    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