BEUDAMED
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    FDA 510(k)
    FDA Class 2 ·Radiology

    Masel

    FDA UDI
    Ortho Organizers, Inc.·00190707041151·Choice™ Weingart Pliers

    ProLift

    FDA UDI
    Life Spine, Inc.·00190837106522·Static Expandable Cage Trial, 10mm x 28mm x 16m...

    ELECSYS PRECICONTROL UNIVERSAL

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    EMG SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    AESCULAP SURGICAL INSTRUMENTS

    FDA Adverse Event
    Injury ·CHRISTOPH MIETHKE GMBH & CO. KG·Product code JXG·November 27, 2019

    AESCULAP SURGICAL INSTRUMENTS

    FDA Adverse Event
    Injury ·CHRISTOPH MIETHKE GMBH & CO. KG·Product code JXG·November 27, 2019

    SPECTRA WAVEWRITER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·August 22, 2024

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Injury ·RICE CREEK MFG·Product code LWP·June 7, 2013

    VITALITY 2

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 6, 2011

    PAINNOT

    FDA Adverse Event
    Injury ·WEIGI INTERNATIONAL CO. LTD.·Product code IRT·September 4, 2008

    ProScreen 10 Panel Dip Card w/Adult, Item No. PSDA-10MO, PSDA-10MMO300, PSDA-10PPX, PSDA-10BUP, PSD-12BUP, PSD-10M, PSCupA-6MB-W, PSCup-10MMO300, PSD-5AB, PSD-10CMO3, PSCupA-10MO, PSCupA-12M-W I-DXA-1127-023, PSCupA-12TBU.

    FDA Enforcement
    Class III ·Terminated·Ameditech Inc·December 30, 2015

    Medical Linear Accelerator

    FDA Enforcement
    Class II ·Terminated·Elekta, Inc.·September 14, 2016