BEUDAMED
    7 results · 20ms · Sources: EU EUDAMED, US FDA

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    CIRCLE NEPHROSTOMY TUBE INTRODUCER

    FDA 510(k)
    FDA Class 1 ·Gastroenterology, Urology

    STRYKER PATIENT SPECIFIC CUTTING GUIDE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BIOSLING - BIOABSORBABLE POLYMER SLING & SURGICAL MESH

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

    EON

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL NEUROMODULATION·Product code GZB·May 6, 2014

    VIRTUOSO VR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code LWS·October 31, 2012

    TECNIS MULTIFOCAL

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code MFK·August 21, 2010

    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