BEUDAMED
    10 results · 26ms · Sources: EU EUDAMED, US FDA

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    THORA-DRAIN(R) ABT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Patterson

    FDA UDI
    PATTERSON DENTAL SUPPLY, INC.·D6620708716241·FILE, PULP CANAL, ENDODONTIC

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867313323·Low Profile Screw, 1.6 x 24mm, Cortical

    IXOS Radius Plate System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EVERELIFE TRANSCUTANEOUS MUSCLE STIMULATOR

    FDA 510(k)
    FDA Class 2 ·Neurology

    TFNA FENESTRATED HELICAL BLADE 95MM

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HSB·April 5, 2021

    TERUMO STERNAL SAW II

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code GFA·April 16, 2014

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·December 13, 2012

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 26, 2015

    SPRYSTEP VECTOR, Custom made device dynamic ankle-foot orthosis (AFO) , Reference numbers: 17V1030, 17V2030, 17V1031, 17V2031, 17V1032, 17V2032, 17V1033, 17V2033, 17V1035, 17V2035, 17V1036, 17V2036, 17V1037, 17V2037

    FDA Enforcement
    Class II ·Completed·Townsend Design·January 17, 2024