BEUDAMED
    9 results · 24ms · 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 ×

    In2Bones Fracture and Correction System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486003616·MCK FEMORAL TRIAL (SIZE 8 RM/LL)

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707018803·CALIBRA 1ST MOLAR BANDS n.LL 18

    Responsive Orthopedics Total Knee Arthroplasty System

    FDA UDI
    RESPONSIVE ORTHOPEDICS, LLC·00841973107477·TRIAL 90-SRK-170518 POLY UCCS 5X18MM

    INSTRUMED VESSEL DILATORS, MODEL 65-7XX,65-9XXX,66-1XXX,65-7048-65-7054

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    IBAG

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

    T-PAL SPACER APPLICATOR KNOB

    FDA Adverse Event
    Malfunction ·SYNTHES HAGENDORF·Product code LXH·October 14, 2014

    PELVICOL 2 X 4 CM

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY TISSUE SCIENCE LABORATORIES·Product code FTL·June 12, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 21, 2011