BEUDAMED
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    EMIT 2000 QUINIDINE ASSAY, MODEL OSR4Q229

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040009437·Zirlux 16+ B1 coloring liquid

    N/A

    FDA UDI
    Smith & Nephew, Inc.·03596010054050·TRAY STERTION ASCOPIC

    GeoShapes™ Elastics

    FDA UDI
    Ortho Organizers, Inc.·00190707097417·GeoShapes™ Elastics 3/8" (9.53 mm) Extra Heavy ...

    MASEL

    FDA UDI
    Ortho Organizers, Inc.·00190707053895·GeoShapes™ Elastics 3/8" (9.53 mm) Extra Heavy ...

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K0112050·Tap, 7.5 mm

    CONTACT DETACH

    FDA Adverse Event
    Injury ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·November 14, 2025

    ATLAST DATA MANAGEMENT SOFTWARE (DMS)

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    PURE WATER SOLUTIONS CENTRAL WATER SYSTEM FOR HEMODIALYSIS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Acapella One

    FDA UDI
    Choice Spine, LP·10885862244796·

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC.·Product code LFR·May 16, 2007

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·March 19, 2013

    ACCU-CHEK ® COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·March 9, 2011

    Argon Medical Devices, ArgoGuide Hydrophilic NiTi Guidewire, K011905, Catalog Number: 00-AG387307, .035/150cm, stiff/straight/standard, sold as a single hydrophilic guidewire in both sterile and bulk non-sterile packaging configurations. Argon Medical Devices, Inc. Athens, TX 75751

    FDA Recall
    Terminated ·Argon Medical Devices, Inc·Product code DQX·November 19, 2007

    Argon Medical Devices, ArgoGuide Hydrophilic NiTi Guidewire, K011905, Catalog Number: 00-AG387312, .035/300cm, stiff/angled/standard, sold as a single hydrophilic guidewire in both sterile and bulk non-sterile packaging configurations. Argon Medical Devices, Inc. Athens, TX 75751

    FDA Recall
    Terminated ·Argon Medical Devices, Inc·Product code DQX·November 19, 2007

    Argon Medical Devices, ArgoGuide Hydrophilic NiTi Guidewire, K011905, Catalog Number: 00-AG087312, .035/300cm, stiff/angled/standard, sold as a single hydrophilic guidewire in both sterile and bulk non-sterile packaging configurations. Argon Medical Devices, Inc. Athens, TX 75751

    FDA Recall
    Terminated ·Argon Medical Devices, Inc·Product code DQX·November 19, 2007

    Argon Medical Devices, ArgoGuide Hydrophilic NiTi Guidewire, K011905, Catalog Number: 00-AG387320, .038/180cm, stiff/straight/standard, sold as a single hydrophilic guidewire in both sterile and bulk non-sterile packaging configurations. Argon Medical Devices, Inc. Athens, TX 75751

    FDA Recall
    Terminated ·Argon Medical Devices, Inc·Product code DQX·November 19, 2007

    Argon Medical Devices, ArgoGuide Hydrophilic NiTi Guidewire, K011905, Catalog Number: 00-AG387324, .038/300cm, stiff/angled/standard, sold as a single hydrophilic guidewire in both sterile and bulk non-sterile packaging configurations. Argon Medical Devices, Inc. Athens, TX 75751

    FDA Recall
    Terminated ·Argon Medical Devices, Inc·Product code DQX·November 19, 2007

    Argon Medical Devices, ArgoGuide Hydrophilic NiTi Guidewire, K011905, Catalog Number: 00-AG387311, .035/180cm, stiff/angled/standard, sold as a single hydrophilic guidewire in both sterile and bulk non-sterile packaging configurations. Argon Medical Devices, Inc. Athens, TX 75751

    FDA Recall
    Terminated ·Argon Medical Devices, Inc·Product code DQX·November 19, 2007

    Argon Medical Devices, ArgoGuide Hydrophilic NiTi Guidewire, K011905, Catalog Number: 00-AG387309, .035/300cm, stiff/straight/standard, sold as a single hydrophilic guidewire in both sterile and bulk non-sterile packaging configurations. Argon Medical Devices, Inc. Athens, TX 75751

    FDA Recall
    Terminated ·Argon Medical Devices, Inc·Product code DQX·November 19, 2007