BEUDAMED
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    CAPIOX RX25 HOLLOW FIBER OXYGENATOR W/WO HARDSHELL RESERVOIR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ImarC™

    FDA UDI
    Carbon Medical Technologies, Inc.·00858015005455·Tissue Marker System - Stereotactic Delivery

    Varex Imaging

    FDA UDI
    Varex Imaging Nederland B.V.·08718755001297·This is a set consisting out of an AEC sensor f...

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690125495·Modular Knee Stem Pilot 21mm x 100mm

    neoWave LS

    FDA UDI
    XENIX MEDICAL LLC·00818345023932·PADDLE SPREADER, 10MM

    Mariner Outrigger

    FDA UDI
    Seaspine Orthopedics Corporation·10889981175436·Z-Rod, Dia. 5.5mm, Co-Cr, 210mm

    Gorilla Plating System

    FDA UDI
    Paragon 28, Inc.·00889795009654·BOW & Arrow, Evans Plate, 10mm Wedge

    DRIVEMEDICAL

    FDA UDI
    Drive Devilbiss Healthcare·50822383525162·Canes & CrutchesCrutches Product Description: E...

    InTess Lumbar Cage

    FDA UDI
    Kalitec Direct LLC·B07312K0102100·Shaver, Open 10mm

    CONTROL MODULE ALGORITHM ENHANCEMENT FOR THE MODEL S500-ST AND MODEL S400

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

    MODIFICATION TO MODEL 5866-37M LEAD ADAPTOR KIT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Specials

    FDA UDI
    Seaspine Orthopedics Corporation·10889981173548·Trial LTL, 13x12x10mm, Flat 7 Deg

    LYNX

    FDA UDI
    HNM TOTAL RECON LLC·00841742110608·LYNX ø3.5mm Std Cortical Screw, Full Thread, Se...

    B-P TOTAL SHOULDER SYSTEM

    FDA UDI
    ENDOTEC, INC.·00814193025388·B-P SHOULDER HUMERAL STEM W/O HEAD W/ ULTRACOAT...

    TESS GLENOID REVERSE HEAD DIAMETER 36

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·October 27, 2016

    Optetrak Logic

    FDA UDI
    Exactech, Inc.·10885862158208·

    RADICAL

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·April 16, 2015

    LOGIC KNEE COMPONENTS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·March 4, 2026

    J-VAC RESERVOIR

    FDA Adverse Event
    Malfunction ·ETHICON, INC·Product code KOG·April 8, 2013

    INSORB SUBCUTICULAR STAPLER

    FDA Adverse Event
    Other ·INCISIVE SURGICAL·Product code GDW·March 25, 2011