BEUDAMED
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    OPHTHALMIC SPECTACLE LENS BLANKS

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    X-Box

    FDA UDI
    INNO Holdings, Inc.·M71188812250·PEEK, Ta

    Snowden-Pencer

    FDA UDI
    CAREFUSION 2200, INC·10885403151842·Snowden-Pencer RETRACTOR DINGMAN MOUTH GAG

    dentaform®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011881225180·dentaform® Snap Band, Tooth 36, Size 25/Roth 18

    LinkSymphoKnee - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575307715·Knee tibia prosthesis trial - LinkSymphoKnee Sy...

    dentaform®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011881225220·dentaform® Snap Band, Tooth 36, Size 25/Roth 22

    dentaform®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011881225000·dentaform® Snap Band, Tooth 36, Size 25

    LinkSymphoKnee - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575307944·Knee tibia prosthesis trial - LinkSymphoKnee Sy...

    LinkSymphoKnee - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575308262·Knee tibia prosthesis trial - LinkSymphoKnee Sy...

    LinkSymphoKnee - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575308095·Knee tibia prosthesis trial - LinkSymphoKnee Sy...

    NA

    FDA UDI
    STRYKER CORPORATION·07613327063820·Cysto Visual Obturator, 25 Fr.

    CARDICA PAS-PORT PROXIMAL ANASTOMOSIS SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ALTAPORE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MANUAL ORTHOPEDIC SURGICAL INSTRUMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code LXH·October 6, 2010

    DURATA STS OPTIM ACTIVE FIXATION, DF4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL INC., CARDIAC RHYTHM MANAGEMENT D·Product code NVY·January 13, 2014

    TOTAL CARE BARIATRIC BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·November 14, 2012

    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