BEUDAMED
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    REFSTAR PLUS WITH QWIKPATCH EXTERNAL REFERENCE PATCH, MODEL D-1210-03, REFSTAR PLUS CABLE, MODEL M-4700-106

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SURE-SCOPE

    FDA UDI
    OBP CORPORATION·M648C0901200·SINGLE-USE LIGHTED LARYNGOSCOPE SIZE MAC 2

    3-LD Set, SNAP - DIN, UNSHIELDED, A,120"

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828147194·3-LD Set, SNAP - DIN, UNSHIELDED, A,120"

    THUNDERBOLT

    FDA UDI
    Choice Spine, LP·00840996189941·THUNDERBOLT,X-TAB SCREW,5.0X90X120

    THUNDERBOLT

    FDA UDI
    Choice Spine, LP·00840996190541·THUNDERBOLT,X-TAB SCREW,6.0X90X120

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707065630·INTRAORAL ELASTICS 2,5 oz 1/8" brown

    N/A

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036027124·

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319735541·Beebee (Crown & Collar) Wire Cutting Scissors, ...

    MODIFICATION TO EXACTECH ACUMATCH INTEGRATED HIP SYSTEM, M-SERIES HIGH OFF-SET NECK SEGMENT, M-SERIES LOW OFF-SET NECK S

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PRO-TORQ

    FDA 510(k)
    FDA Class 1 ·Dental

    Atropos PTA Balloon Dilatation Catheter

    FDA UDI
    BrosMed Medical Co.,Ltd.·06958481446616·

    Atropos PTA Balloon Dilatation Catheter

    FDA UDI
    BrosMed Medical Co.,Ltd.·06958481448610·

    Minerva PTA Balloon Dilatation Catheter

    FDA UDI
    BrosMed Medical Co.,Ltd.·06958481419825·

    Minerva PTA Balloon Dilatation Catheter

    FDA UDI
    BrosMed Medical Co.,Ltd.·06958481417821·

    Atropos PTA Balloon Dilatation Catheter

    FDA UDI
    BrosMed Medical Co.,Ltd.·06958481447613·

    Minerva PTA Balloon Dilatation Catheter

    FDA UDI
    BrosMed Medical Co.,Ltd.·06958481418828·

    ECHELON*FLEX60 LONG ARTICULATING ENDOSCOPIC LINEAR CUTTER, 60 MM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·May 2, 2013

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·September 15, 2014

    POLYSORB 2 36 VIOLET KV-40

    FDA Adverse Event
    Injury ·UNITED STATES SURGICAL·Product code GAM·May 6, 2011

    UNKNOWN

    FDA Adverse Event
    Injury ·WILLIAM COOK EUROPE·Product code DTK·May 20, 2016