BEUDAMED
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    Sniper (R) Spine System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TMA - Archwire

    FDA UDI
    ORMCO CORPORATION·00889989029611·ARCH TMA REV.CURVE LWR 016X022 PK/10

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694009140·.045 x 4 K-Wire

    LOCATOR F-Tx

    FDA UDI
    Zest Anchors, LLC·00840481124181·LOCATOR F-Tx Abutment for Mini Platform GS Conn...

    LOCATOR R-Tx

    FDA UDI
    Zest Anchors, LLC·00840481123115·LOCATOR R-Tx Attachment System for TS/ET Fixtur...

    MIRABAY

    FDA UDI
    Mirabay Orthodontics Corp.·05061075022606·KLEOS PSL METAL MBT 022 UR45 PK5 UNI

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707016793·CALIBRA 1ST MOLAR BANDS n.LR 3

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 12, 2020

    OHICHO3

    FDA Adverse Event
    Injury ·Product code LIT·July 19, 2019

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 14, 2020

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·September 30, 2020

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·May 28, 2020

    OHICHO3

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·September 26, 2018

    OHICHO3

    FDA Adverse Event
    Injury ·Product code LIT·September 17, 2019

    SETx CERVICAL INTERBODY INSERTER

    FDA UDI
    XENCO MEDICAL LLC·B064XMPH11600031·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694067744·.045" x 4" K-Wire Sterile Qty 5

    MTF NEW BONE VOID FILLER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EXCELART VANTAGE ZGV

    FDA 510(k)
    FDA Class 2 ·Radiology

    Stent, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·PRO-KINETIC ENERGY COBALT CHROMIUM (CoCr) CORONARY STENT SYSTEM

    Stent, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·PRO-Kinetic Energy Coronary Stent System