BEUDAMED
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    Canon non-mydriatic retinal camera CR series

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    MULTI-GUIDE

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·04546540257772·SINGLE DRILL GUIDE INSERT

    36M - Black & Veach - Metal

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588011820·36M - Black & Veach - Metal

    OneLIF™

    FDA UDI
    Novapproach Spine LLC·G07001332011220·Retention Plate, Anterior-Only, Large, 11 mm - ...

    VANISH POINT

    FDA Adverse Event
    Malfunction ·RETRACTABLE TECHNOLOGIES, INC.·Product code MEG·April 6, 2021

    BENZ-G 4X (HIOXIFILCON D) MULTIFOCAL LATHED LENS

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    PROLENE SOFT (POLYPROPYLENE), NONABSORBABALE SYNTHETIC SURGICAL MESH

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

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523124015·Tibial cutting block L-5°

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523100910·L Tibial Baseplate Cemented Stemmed Sz 6

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523100880·L Tibial Baseplate Cemented Stemmed Sz 3

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523100927·L Tibial Baseplate Cemented Stemmed Sz 7

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523100934·L Tibial Baseplate Cemented Stemmed Sz 8

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523100903·L Tibial Baseplate Cemented Stemmed Sz 5

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523100897·L Tibial Baseplate Cemented Stemmed Sz 4

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523124008·Tibial Saw Block Zero Slope Left

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523100873·L Tibial Baseplate Cemented Stemmed Sz 2

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523100866·L Tibial Baseplate Cemented Stemmed Sz 1

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523100859·L Tibial Baseplate Cemented Stemmed Sz 0

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·May 15, 2022

    UNKNOWN OPTEASE VENA CAVA FILTER

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code DTK·August 11, 2011