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    HOYA SURGICAL OPTICS, INC.

    FDA registration
    HOYA SURGICAL OPTICS, INC.·2 products·🇺🇸 United States

    ISERT ASPHERIC INTRAOCULAR LENS

    FDA Adverse Event
    Malfunction ·HOYA SURGICAL OPTICS INC.·Product code HQL·January 15, 2010

    ISERT ASPHERIC INTRAOCULAR LENS

    FDA Adverse Event
    Malfunction ·HOYA SURGICAL OPTICS, INC.·Product code HQL·January 6, 2011

    ISYMM ASPHERIC INTRAOCULAR LENS

    FDA Adverse Event
    Injury ·HOYA SURGICAL OPTICS INC.·Product code HQL·August 28, 2009

    ISERT ASPHERIC INTRAOCULAR LENS

    FDA Adverse Event
    Malfunction ·HOYA SURGICAL OPTICS, INC.·Product code HQL·February 19, 2010

    ISERT ASPHERIC INTRAOCULAR LENS

    FDA Adverse Event
    Malfunction ·HOYA SURGICAL OPTICS INC.·Product code HQL·January 12, 2011

    ISYMM ASPHERIC INTRAOCULAR LENS

    FDA Adverse Event
    Injury ·HOYA SURGICAL OPTICS, INC.·Product code HQL·September 16, 2009

    ISYMM ASPHERIC INTRAOCULAR LENS

    FDA Adverse Event
    Injury ·HOYA SURGICAL OPTICS INC.·Product code HQL·September 16, 2009

    ISYMM ASPHERIC INTRAOCULAR LENS

    FDA Adverse Event
    Malfunction ·HOYA SURGICAL OPTICS INC.·Product code HQL·July 17, 2009

    HOYA-IS INJECTOR SYSTEM

    FDA Adverse Event
    Malfunction ·HOYA SURGICAL OPTICS INC.·Product code MSS·October 28, 2010

    ISYMM ASPHERIC INTRAOCULAR LENS

    FDA Adverse Event
    Malfunction ·HOYA SURGICAL OPTICS INC.·Product code HQL·December 18, 2009

    iSert Intraocular Lens (Model PC-60AD)

    FDA Recall
    Terminated ·Hoya Surgical Optics, Inc.·Product code HQL·June 17, 2011

    iSymm Intraocular Lens (Model FC-60AD) The Hoya iSymm Model FC-60AD Intraocular Lens (IOL) is an ultraviolet-light absorbing posterior chamber intraocular lens designed to be implanted posterior to the iris where the lens will replace the optical function of the natural crystalline lens. However, accommodation will not be replaced. The optic of this lens is designed to produce negative spherical aberration. The Hoya iSymm Model FC-60AD Intraocular Lens is indicated for primary implantation in the capsular bag of the eye for the visual correction of aphakia in adult patients in whom a cataractous lens has been removed.

    FDA Recall
    Terminated ·Hoya Surgical Optics, Inc.·Product code HQL·June 17, 2011

    ISERT 231

    FDA Adverse Event
    Injury ·HOYA SURGICAL OPTICS, INC.·Product code HQL·November 18, 2015

    ISERT 251

    FDA Adverse Event
    Injury ·HOYA SURGICAL OPTICS, INC.·Product code HQL·November 18, 2015

    ISERT 231

    FDA Adverse Event
    Injury ·HOYA SURGICAL OPTICS, INC.·Product code HQL·November 18, 2015

    ISERT 251

    FDA Adverse Event
    Injury ·HOYA SURGICAL OPTICS, INC.·Product code HQL·November 18, 2015

    ISERT 231

    FDA Adverse Event
    Injury ·HOYA SURGICAL OPTICS, INC.·Product code HQL·November 18, 2015

    ISERT 231

    FDA Adverse Event
    Injury ·HOYA SURGICAL OPTICS, INC.·Product code HQL·November 18, 2015

    ISERT 231

    FDA Adverse Event
    Injury ·HOYA SURGICAL OPTICS, INC.·Product code HQL·November 18, 2015