BEUDAMED
    7 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.
    Filters Regulation: Us FDA ×

    CAVITY DRAINAGE CATHETERIZATION SET, CS-01600

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690197584·AK3 PS-R Insert Trial Size 5, 16mm

    C-89 GOLD BASE DENTAL ALLOY

    FDA 510(k)
    FDA Class 2 ·Dental

    CANDELA PLDL-1 PULSED DYE LASER

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·June 25, 2014

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·January 3, 2013

    ZIRCONIA

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC. BROOKS MANUFACTURING SITE·Product code LZO·November 10, 2010