BEUDAMED
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    PILLING LACRIMAL INTUBATION SYSTEM

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    nextaro Transfer System, nextaro va

    FDA 510(k)
    FDA Class 2 ·General Hospital

    AVIVO MOBILE PATIENT MANAGEMENT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACCU-CHEK ® MULTICLIX

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·May 15, 2014

    REVO MRI SURESCAN

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code LWP·October 31, 2012

    DURASTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FPO·August 18, 2010

    Zeiss brand IOLMaster, Version 1-5, Biomicroscope, Slit-Lamp, AC-Powered, Product is manufactured by Carl Zeiss Meditec AG (Jena), Carl Zeiss Promenade 10, Jena, Germany 07745; and distributed by Carl Zeiss Meditec, Inc., Dublin, CA This device is intended for use primarily by physicians and health care workers and may be only used under the supervision of a physician. This device will not be sold to the general public. The IOLMaster is intended for the biometric determination of ocular measurements of axial length, anterior chamber depth, corneal radius, white-to white (WTW), and for the measurement of pupil size and deviation of the visual axis from the center of the pupil. For patients who are candidates for intraocular lens (IOL) implantation, the device also performs calculations to assist physicians in determining the appropriate IOL power and type for implantation

    FDA Enforcement
    Class II ·Terminated·Carl Zeiss Meditec, Inc.·November 27, 2013