BEUDAMED
    8 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    NK DIGI-GRIP SENSOR, MODEL DGR001

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    KITS AND TRAYS FOR ONE TIME USE ONLY

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    ADHOC CLAW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BIVONA-PORTEX

    FDA Adverse Event
    Injury ·SMITHS MEDICAL·Product code JOH·December 9, 2010

    PINNACLE 100 ACET CUP 54MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·January 22, 2013

    TENDRIL ST

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 9, 2014

    ACDF MECTA-C SA DRILL SCREW LOCK 3.8X14 (2X)

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code OVE·March 31, 2021

    ev3 Pipeline Flex Embolization Device. For neurological endovascular use.

    FDA Enforcement
    Class I ·Terminated·Micro Therapeutics Inc, Dba Ev3 Neurovascular·April 1, 2020