BEUDAMED
    8 results · 27ms · 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 ×

    SYNTHES(USA) SYNTHES HYBRID EXTERNAL FIXATOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LARGE EX-FIX 11MM CRBN FBR ROD 250MM / MR-CONDITIONAL

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code KTT·April 12, 2018

    LARGE EX-FIX 11MM CRBN FBR ROD 300MM / MR-CONDITIONAL

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code KTT·April 12, 2018

    KAPP BARI-RING, MODEL KS-BR-2005

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

    IPL400

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

    TREK CORONARY DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code LOX·February 8, 2013

    EON 16-CHANNEL IPG

    FDA Adverse Event
    Malfunction ·SJM NEUROMODULATION DIVISION·Product code LGW·December 14, 2010

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 22, 2014