BEUDAMED
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    MaxLock

    FDA UDI
    TORNIER, INC.·00846832043941·MXK COMPRESSOR/DISTRACTOR

    MaxLock

    FDA UDI
    TORNIER, INC.·00846832043910·K-WIRE

    HEARTSTART SLA BATTERY

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code DQA·November 26, 2014

    ALLEGRO OCULYZER

    FDA Adverse Event
    Malfunction ·WAVELIGHT GMBH·Product code MXK·October 20, 2017

    ALLEGRO OCULYZER

    FDA Adverse Event
    Malfunction ·WAVELIGHT GMBH·Product code MXK·October 23, 2017

    OCULUS PENTACAM

    FDA Adverse Event
    Malfunction ·OCULUS OPTIKGERATE GMBH·Product code MXK·November 7, 2025

    ALLEGRO OCULYZER

    FDA Adverse Event
    Malfunction ·WAVELIGHT GMBH·Product code MXK·September 22, 2020

    ALLEGRO OCULYZER

    FDA Adverse Event
    Malfunction ·WAVELIGHT GMBH·Product code MXK·May 1, 2013

    ORBSCAN

    FDA Adverse Event
    Injury ·Product code MXK·October 9, 2010

    GALILEI G6 LENS PROFESSIONAL

    FDA Adverse Event
    Injury ·SIS LTD., SURGICAL INSTRUMENT SYSTEMS·Product code MXK·June 8, 2020

    WAVELIGHT OCULYZER II DIAGNOSTIC DEVICE

    FDA Adverse Event
    Malfunction ·WAVELIGHT GMBH·Product code MXK·September 26, 2024

    ALLEGRO OCULYZER

    FDA Adverse Event
    Malfunction ·WAVELIGHT GMBH·Product code MXK·August 27, 2018

    ALLEGRO OCULYZER

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code MXK·June 7, 2018

    ALLEGRO OCULYZER

    FDA Adverse Event
    Malfunction ·WAVELIGHT GMBH·Product code MXK·December 16, 2019

    ALLEGRO OCULYZER

    FDA Adverse Event
    Malfunction ·WAVELIGHT GMBH·Product code MXK·November 27, 2019

    Oculus Pentacam AXL Wave, Ref 70020, CE 0123

    FDA Recall
    Open, Classified ·Oculus Optikgeraete GMBH Munchholzhauser Str. 29 Wetzlar Germany·Product code MXK·August 8, 2023

    Pentacam HR REF 70900. Used to image the anterior segment of the eye.

    FDA Recall
    Open, Classified ·Oculus Optikgeraete GMBH Munchholzhauser Str. 29 Wetzlar Germany·Product code MXK·July 8, 2022

    Oculus Pentacam AXL , Ref 70100, CE 0123

    FDA Recall
    Open, Classified ·Oculus Optikgeraete GMBH Munchholzhauser Str. 29 Wetzlar Germany·Product code MXK·August 8, 2023

    Oculus Myopia Master , Ref 68100, CE 0123

    FDA Recall
    Open, Classified ·Oculus Optikgeraete GMBH Munchholzhauser Str. 29 Wetzlar Germany·Product code MXK·August 8, 2023

    Pentacam AXL Wave REF 70020. Used to image the anterior segment of the eye.

    FDA Recall
    Open, Classified ·Oculus Optikgeraete GMBH Munchholzhauser Str. 29 Wetzlar Germany·Product code MXK·July 8, 2022