BEUDAMED
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    GALAXY

    FDA 510(k)
    FDA Class 2 ·Dental

    Alleset

    FDA UDI
    GRI Medical & Electronic Technology Co., Ltd.·16931918184418·Needle Counter_30-Count_Double Magnet_N/S_100ea/cs

    SBi

    FDA UDI
    Provision·B504OM10030070·

    Medical Facets NC

    FDA UDI
    MEDICAL FACETS NC LLC·M933MDF20030070·1.5mm Cortex Screw, 1.5 Hex, Self-Tapping, 7mm

    BIOTRANS™ Reusable Sensor Base and Monitor Adapter Cables

    FDA UDI
    BIOPTIMAL INTERNATIONAL PTE. LTD.·08886483506947·

    BIOTRANS™ Reusable Sensor Base and Monitor Adapter Cables

    FDA UDI
    BIOPTIMAL INTERNATIONAL PTE. LTD.·08888893501314·

    Diamondback Peripheral

    FDA UDI
    Cardiovascular Systems, Inc.·10852528005879·Diamondback Peripheral, Exchangeable Series, 1....

    SULZER VASCUTEK GELSOFT ERS VASCULAR PROSTHESIS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    IMMULITE CARBAMAZEPINE, IMMULITE 2000 CARBAMAZEPINE, CATALOG # LKCB1, LKCB5 & L2KCB2, L2KCB6

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    CHARNLEY OGEE CUP 22.225/40MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·February 13, 2004

    ANTERIOR CHAMFER REAMER

    FDA Adverse Event
    Malfunction ·STRYKER GMBH·Product code HTO·November 1, 2018

    SOLETRA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·September 25, 2013

    KINETRA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·October 24, 2012

    SOLETRA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·September 25, 2013

    KINETRA

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code MHY·February 16, 2012

    KURZ UPPER EYELID IMPLANT- PLATINUM/IRIDIUM,MODELS REGULAR 4007 003-007, SPECIAL 4007 002, 4007 008-010

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    RX VIATRAC 14 PERIPHERAL DILATATION CATHETER, MODEL #'S 1003006-20, 1003007-20, 1003008-20, 1003009-20, 1003010-20, 1003

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RENAISSANCE 26 OBS 10/25/04

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FPO·March 13, 2013

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·February 28, 2011

    D-TRONPLUS

    FDA Adverse Event
    Injury ·DISETRONIC MEDICAL SYSTEMS·Product code LZG·February 22, 2008