BEUDAMED
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    STERILE SURGEONS' GLOVES

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867130166·2.4MM VAL DRILL GUIDE, FOR DRP

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·June 19, 2024

    ChoiceSpine Octane A/T/P Spinal Implant System, ChoiceSpine Cervical Interbody Spacer System Ascendant PC, ChoiceSpine Cervical Interbody Spacer System Ascendant, ChoiceSpine Cervical Spacer System Blackhawk, ChoiceSpine Intervertebral Fusion Device Octane Straight, ChoiceSpine Intervertebral Fusion Device Octane Straight PC, ChoiceSpine VEO Laterial Access & Interbody Fusion System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MANNITOL SALT AGAR

    FDA 510(k)
    FDA Class 1 ·Microbiology

    RESTORE ULTRA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·June 24, 2014

    ACRYSOF

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·October 20, 2010

    CONSTELLATION VISION SYSTEM

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·December 7, 2012

    VOLAR DISTAL RAD PLT TI NARROW RT 3H

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HRS·June 9, 2020

    VOLAR DISTAL RAD PLT TI STD RT 5H

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HRS·June 9, 2020