BEUDAMED
    7 results · 22ms · 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 ×

    densitas densityai

    FDA 510(k)
    FDA Class 2 ·Radiology

    DISPOSABLE AND REUSABLE CONCENTRIC NEEDLES / DISPOSABLE AND REUSABLE MONOPOLAR NEEDLE

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    SILVER DENTAL ARREST

    FDA 510(k)
    FDA Class 2 ·Dental

    MOUNTAINEER 31MM OC PLATE

    FDA Adverse Event
    Malfunction ·DEPUY SPINE, INC.·Product code KWP·July 21, 2011

    PFNA-II BLADE L90 TAN

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code KTT·June 27, 2013

    MECHANICAL CHAIR/TRANSPORT CHAIR

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code IOR·October 22, 2014

    Allura Exper FD Series. System codes 722003 722010 722022 722005 722011 722019 722001 722002 722006 722012 722008 722013 722020 722025 722015 722023 722038 889006 889016 889009 722005 The device is an X-Ray Generator.

    FDA Enforcement
    Class II ·Terminated·Philips North America, LLC·March 25, 2020