BEUDAMED
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    TS FIXTURE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    ArgenZ HT+ 98x12 A4

    FDA UDI
    ARGEN CORPORATION, THE·D818121995·Dental porcelain/ceramic restoration kit

    ESCAPE CONTROL MODULE

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    CAPNOSTREAM 20P WITH MASIMO SPO2 BOARD

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    STERNGOLD IMPLAMED, FIXTURE, TI,

    FDA Adverse Event
    Injury ·STERNGOLD IMPLAMED·Product code DZE·February 16, 1998

    GENESIS

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC./ORTHOPAEDICS DIV·Product code HSH·November 16, 1998

    ZY PACING LEAD

    FDA Adverse Event
    Death ·SULZER OSCOR INC.·Product code DTB·July 13, 1998

    BD INSULIN SYRINGE WITH THE BD ULTRA-FINE¿ NEEDLE 0.5ML 31GX5/16 (8MM)

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·September 12, 2017

    UNK

    FDA Adverse Event
    Other ·SAFESKIN CORP.·Product code LYY·January 13, 1999

    UNK

    FDA Adverse Event
    Injury ·ANSELL PERRY·Product code LYY·November 25, 1997

    CCD SPINAL FIXATION SYSTEM

    FDA Adverse Event
    Injury ·SOFAMOR DANEK EUROPE·Product code JDN·February 4, 2000

    95 DEGREE DCS PLATE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KWQ·August 4, 1998

    ZYDERM 1 COLLAGEN IMPLANT

    FDA Adverse Event
    Injury ·COLLAGEN CORP.·Product code LMH·March 13, 1998

    Micropuncture

    FDA UDI
    COOK INCORPORATED·00827002116979·Micropuncture, Introducer Set With Stainless St...

    Micropuncture

    FDA UDI
    COOK INCORPORATED·00827002098893·Micropuncture, Introducer Set With Stainless St...

    INFINION? CX

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·April 11, 2026

    LINEAR? ST

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·July 30, 2025

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·May 21, 2013

    HALO90 ABLATION CATHETER

    FDA Adverse Event
    Other ·BARRX MEDICAL INC.·Product code GEI·June 3, 2011

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·August 13, 2008