BEUDAMED
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    DRIDAU OPIATE ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040014202·Zirlux 16+ B2 98.5X22

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613038649·Tissue Forceps, 1 x 2 Teeth, Overall Length 6" ...

    CORINNE MCCORMACK INC.

    FDA UDI
    FGX INTERNATIONAL INC.·00193033243718·

    ELECTROSURGICAL ELECTRODE FAMILY, MODEL 20-2 NEEDLE BALLOON CATHETER, MODEL 40-4 NEEDLE BALLOON CATHETER, MODEL 60-6 NEE

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

    64 CHANNEL EEG / MODEL NUMBER EX-NW-64

    FDA 510(k)
    FDA Class 2 ·Neurology

    MATIRA ANTERIOR CERVICAL SYSTEM

    FDA UDI
    Kalitec Direct LLC·B07307K0111101·AWL, 10MM SPRING LOADED

    MPFL

    FDA UDI
    ORTHOPEDIATRICS CORP.·00841132145296·3.5MM CANNULATED DRILL, CALIBRATED, TRILOBE DRIVE

    MPFL

    FDA UDI
    ORTHOPEDIATRICS CORP.·00841132145319·3.2MM X 300MM FLARED TIP GUIDE PIN

    MPFL

    FDA UDI
    ORTHOPEDIATRICS CORP.·00841132145333·7MM CANNULATED DRILL, CALIBRATED, TRILOBE DRIVE

    MPFL

    FDA UDI
    ORTHOPEDIATRICS CORP.·00841132145340·3MM - 7MM GRAFT SIZING BLOCK

    MPFL

    FDA UDI
    ORTHOPEDIATRICS CORP.·00841132145289·2.0MM X 150MM FLARED TIP GUIDE PIN

    MPFL

    FDA UDI
    ORTHOPEDIATRICS CORP.·00841132145364·MPFL INSTRUMENT CASE LID

    MPFL

    FDA UDI
    ORTHOPEDIATRICS CORP.·00841132145357·MPFL INSTRUMENT CASE

    MPFL

    FDA UDI
    ORTHOPEDIATRICS CORP.·00841132145326·6MM CANNULATED DRILL, CALIBRATED, TRILOBE DRIVE

    MPFL

    FDA UDI
    ORTHOPEDIATRICS CORP.·00841132145302·4MM CANNULATED TAP

    TITANIUM SCREW LOW PROFILE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBF·November 13, 2020

    M2A 38MM MOD HD+9MM NK NO SKRT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·November 4, 2020

    BI-METRIC/X POR NC 14X150

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·November 4, 2020

    MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·MED-EL ELEKTROMEDIZINISCHE GERAETE, GMBH·Product code MCM·March 15, 2013