BEUDAMED
    6 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 ×

    MTA MATERIAL

    FDA 510(k)
    FDA Class 2 ·Dental

    17HK700G-W

    FDA 510(k)
    FDA Class 2 ·Radiology

    POLYFLEX STENT SYSTEM WITH DELIVERY SYSTEM, MODEL M00514270, M00514280, 00514290, 00514300, 00514310, 00514320, 00514330

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

    NONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code NKB·February 22, 2013

    OCTRODE TRIAL LEAD KIT, 60CM LENGTH

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·February 2, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·August 5, 2014