BEUDAMED
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    XRES BLOOD COLLECTION RESERVOIR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Trial Tibial Augment

    FDA UDI
    ADLER ORTHO SPA·08056269043618·TRIAL PANTHEON TIBIAL AUGMENT LM/RL SIZE 7 H5

    Precisor Broncho

    FDA UDI
    Conmed Corporation·30653405052139·Precisor® Broncho Biopsy Alligator Cup Forceps ...

    EPAD

    FDA UDI
    SAFEOP SURGICAL, INC.·00851641007183·EPAD Cervical Electrodes Pouch Kit

    KITZMILLER COOLEY CLAMP

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896002579·KITZMILLER COOLEY CLAMP ANGLED LEFT

    KITZMILLER COOLEY CLAMP

    FDA UDI
    SONTEC INSTRUMENTS, INC.·B09921005070·KITZMILLER COOLEY CLAMP ANGLED LEFT

    The Orthodontic Store

    FDA UDI
    Young Innovations, Inc.·00843471155677·V Nat D 018 Up

    TALOS®-C HA

    FDA UDI
    MEDITECH SPINE, LLC·B167521005070·

    AMP

    FDA UDI
    ALPHATEC SPINE, INC.·00190376285689·LIF AMP TEMPLATE, 0507

    Indus®

    FDA UDI
    SPINEFRONTIER, INC.·00190361001232·Inset 1 Level ACP, 7mm

    InTess Lumbar Cage

    FDA UDI
    Kalitec Direct LLC·B07312K0105070·Draw Rod, Primal T- Handle

    EVERLIFE INTERFERENTIAL CURRENT THERAPY, MODEL IF-100507

    FDA 510(k)
    FDA Class 2 ·Neurology

    VACUETTE BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·GREINER BIO-ONE NA INC.·Product code JKA·January 9, 2021

    VISTAKON (METHAFILCON A) CONTACT LENSES

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    CAVERMAP SURGICAL AID

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    Young Specialties

    FDA UDI
    Young Innovations, Inc.·00840326425237·NiTi SE Archwire, NAT .018 Upper Dimple 10EA

    AUTOFEED HUMIDIFICATION CHAMBER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE, LTD.·Product code BTT·September 9, 2010

    NC TREK CORONARY DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code LOX·May 8, 2013

    ROTABLATOR ROTATIONAL ATHERECTOMY SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - FREMONT·Product code MCX·May 24, 2011

    CARPENTIER-EDWARDS PERIMOUNT PLUS PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Death ·EDWARDS LIFESCIENCES·Product code LWR·August 5, 2008