BEUDAMED
    7 results · 17ms · Sources: EU EUDAMED, US FDA

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    LINK CEMENT PLUG

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

    PLATFORM SPLINTS

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    AAP BONE PLATES AND SCREW IMPLANTS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    GYNECARE GYNEMESH* PS

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

    MINILINK TRANSMITTER

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code MDS·July 31, 2014

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·January 24, 2011

    OPTETRAK Comprehensive Knee System including OPTETRAK All-polyethylene UNI Tibial Components, Product Lines, 252-12-XX, 252-13-XX, 252-22-XX, 252-23-XX. NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.

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