BEUDAMED
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    MEMOGRAPH; OSSTAPLE - ORAL AND MAXILLIOFACIAL PROCEDURES FOR THE MEMOGRAPH STAPLE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    BiOM T2

    FDA UDI
    BIONX MEDICAL TECHNOLOGIES, INC.·B15520012190·BiOM T2 Wireless Tuning Device

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092001219·artVeneer life lower anteriors, UCM, B2

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180179417·GORNEY FACE LIFT TC-SCISSORS, STRAIGHT 19CM

    Creation Willi Geller

    FDA UDI
    KLEMA Dentalprodukte GmbH·ECWG0012191·Magic Colour Glaze

    Creation Willi Geller

    FDA UDI
    KLEMA Dentalprodukte GmbH·09010782022207·Magic Colour Glaze

    Alleset

    FDA UDI
    GRI Medical & Electronic Technology Co., Ltd.·16931918195865·Radial Femoral Angiography Drape_4 fenestrated_...

    LIFEPAK® 15 monitor/defibrillator

    FDA UDI
    PHYSIO-CONTROL, INC.·00883873912775·15AAEBABBABBBBAAAAAAAAABLP15 MONITOR/DEFIB

    TI500 GLOBE-TROTTER TRANSPORT SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ROVERS ENDOCERVEX-BRUSH

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523163151·4 Hole Speed Guide, 19mm

    Sonova Brand (multiple brand)

    FDA UDI
    Sonova AG·07613389402568·Easy Line Remote 2.0 app

    BD DISCARDIT II 10 ML SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·June 2, 2020

    INTACS PRESCRIPTION INSERTS

    FDA Adverse Event
    Injury ·ADDITION TECHNOLOGY, INC.·Product code LQE·June 20, 2006

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·June 11, 2025

    IMPAX CV REPORTING

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP·Product code LLZ·February 26, 2013

    CONCERTO CRT-D DR

    FDA Adverse Event
    Death ·MEDTRONIC MED REL, INC.·Product code NIK·February 24, 2011

    COMPAX 40E

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS, LLC·Product code IZZ·February 22, 2008

    INTACS PRESCRIPTION INSERTS

    FDA Adverse Event
    Injury ·ADDITION TECHNOLOGY, INC.·Product code LQE·April 3, 2006

    INTACS CORNEAL IMPLANTS

    FDA Adverse Event
    Injury ·ADDITION TECHNOLOGY, INC.·Product code LQE·June 20, 2006