BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    Acumed Acutrak 3 Headless Compression Screw System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LIGASURE 5MM BLUNT TIP LAPAROSCOPIC SEALER/DIVIDER

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

    BLACKSTONE SURGICAL TITANIUM MESH

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LONG NAIL KIT R1.5, LEFT 10X260MM X 125

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·June 16, 2010

    INTERJECT INJECTION THERAPY NEEDLE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FCG·October 28, 2008

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·September 1, 2011

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 17, 2013

    OPTETRAK Comprehensive Knee System including OPTETRAK Logic RBK PS Tibial Components (Product Line: 02-012-38-XXXX). NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·October 13, 2021