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 ×

    HI DENSE TC

    FDA 510(k)
    FDA Class 2 ·Dental

    IRON SET, ITEM NO. 65008

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    MODIFICATION TO VERTEBROPLASTIC RADIOPAQUE BONE CEMENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code PAH·February 21, 2013

    PRECICE® INTRAMEDULLARY LIMB LENGTHENING ROD

    FDA Adverse Event
    Injury ·ELLIPSE TECHNOLOGIES, INCORPORATED·Product code HSB·July 31, 2014

    FIXODENT DENTURE ADHESIVE, VERSION UNKNOWN (CALCIUM ZINC GANTREZ SALT 33%, CELLU

    FDA Adverse Event
    Other ·PROCTER & GAMBLE MANUFACTURING CO.·Product code KOO·January 24, 2011

    KLS Martin Cranial Implants - MR Conditional; K944565: KLS-Martin Micro Osteosynthesis System (1.5MM); K971297: KLS Martin Centre-Drive Drill-Free Screw; K060177: KLS Martin Rigid Fixation - Sterile; K062570: Individual Patient Solutions - Ti (IPS-Ti); K072707: Individual Patient Solutions - PEEK (IPS-PEEK) ; K151382: Individual Patient Solutions - (IPS-PEEK) - STERILE

    FDA 510(k)
    FDA Class 2 ·Neurology