BEUDAMED
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    SAS SPICER-EDWARDS EN COMPLEX ANTISERUM

    FDA 510(k)
    FDA Class 2 ·Microbiology

    3M™ Victory Series™

    FDA UDI
    3M UNITEK CORPORATION·00652221118226·3M™ Victory Series™ Second Molar Bands, 955-227...

    GLUCOSE (HK) REAGENT, UNIVERSAL

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    MICRO-EIA THEOPHYLLINE TEST KIT MONOCLONAL

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    PINN CAN BONE SCREW 6.5MMX20MM

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDICS·Product code NDJ·February 11, 2013

    EPIC PLUS DR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·January 10, 2011

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·July 24, 2014

    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