BEUDAMED
    5,349 results · 31ms · Sources: EU EUDAMED, US FDA

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    INTRAOCULAR PRESSURE LOWERING IMPLANT

    FDA Adverse Event
    Injury ·GLAUKOS CORPORATION·Product code OGO·June 20, 2019

    Glaucoma Aqueous Shunt, 209 mm, valved, P/N EG209V

    FDA Recall
    Terminated ·Eagle Vision Inc·Product code KYF·April 12, 2006

    Valve-EV Glaucoma Ultra-Smooth, P/N 6006

    FDA Recall
    Terminated ·Eagle Vision Inc·Product code KYF·April 12, 2006

    XEN Gel Stent, REF 5513-001(US Model), Sterile, RX Only, (01)10888628032439 ; Other Model Numbers: 5507-001(Global Model) and 5517-001(Australia model) Implant for glaucoma treatment.

    FDA Recall
    Open, Classified ·Allergan PLC·Product code KYF·October 30, 2019

    Glaucoma Aqueous Shunt 365 mm, valved, P/N EG365V

    FDA Recall
    Terminated ·Eagle Vision Inc·Product code KYF·April 12, 2006

    Molteno3 Glaucoma Implants G-Series: GS-Single Plate 175mm2 (IOP reorder#: M3-175) GL-Single Plate 230mm2 (IOP reorder#: M3-230)

    FDA Recall
    Terminated ·Innovative Ophthalmic Products, Inc·Product code KYF·February 22, 2016

    Krupin Eye Valve, P/N 6003

    FDA Recall
    Terminated ·Eagle Vision Inc·Product code KYF·April 12, 2006

    AHMED GLAUCOMA VALVE

    FDA Adverse Event
    Malfunction ·NEW WORLD MEDICAL, INC·Product code KYF·November 15, 2016

    XEN 45 GTS

    FDA Adverse Event
    Malfunction ·ALLERGAN (IRVINE)·Product code KYF·December 28, 2016

    EX-PRESS GLAUCOMA FILTRATION DEVICE

    FDA Adverse Event
    Injury ·OPTONOL LTD.·Product code KYF·November 18, 2016

    EX-PRESS GLAUCOMA FILTRATION DEVICE

    FDA Adverse Event
    Injury ·OPTONOL LTD.·Product code KYF·November 7, 2016

    BAERVELDT SHUNT

    FDA Adverse Event
    Malfunction ·ABBOTT MEDICAL OPTICS·Product code KYF·December 30, 2016

    EX-PRESS GLAUCOMA FILTRATION DEVICE

    FDA Adverse Event
    Injury ·OPTONOL LTD.·Product code KYF·October 6, 2016

    EX-PRESS GLAUCOMA FILTRATION DEVICE

    FDA Adverse Event
    Injury ·OPTONOL LTD.·Product code KYF·November 21, 2016

    EX-PRESS GLAUCOMA FILTRATION DEVICE

    FDA Adverse Event
    Injury ·OPTONOL LTD.·Product code KYF·August 25, 2015

    EX-PRESS GLAUCOMA FILTRATION DEVICE

    FDA Adverse Event
    Injury ·OPTONOL LTD.·Product code KYF·July 23, 2015

    EX-PRESS GLAUCOMA FILTRATION DEVICE

    FDA Adverse Event
    Injury ·OPTONOL LTD.·Product code KYF·August 4, 2015

    EX-PRESS GLAUCOMA FILTRATION DEVICE

    FDA Adverse Event
    Injury ·OPTONOL LTD.·Product code KYF·July 20, 2015

    EX-PRESS GLAUCOMA FILTRATION DEVICE

    FDA Adverse Event
    Malfunction ·OPTONOL LTD.·Product code KYF·August 14, 2015

    AHMED GLAUCOMA VALVE

    FDA Adverse Event
    Malfunction ·NEW WORLD MEDICAL, INC.·Product code KYF·August 21, 2015