BEUDAMED
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    ROYAL MARSDEN GOLD GRAIN GUN

    FDA 510(k)
    FDA Class 1 ·Radiology

    AXSOS

    FDA UDI
    Stryker GmbH·07613327010190·Targeting Tray 5.0mm System

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471156050·K-WIRE - SINGLE TROCAR 1.1mm DIA x 230mm

    PERI-STRIPS STAPLE LINE REINFORCEMENT-SLEEVE CONFIGURATION, PERI-STRIPS STAPLE LINE REINFORCEMENT-STRIP CONFIGURATION

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

    EMERGE MEDICAL PERIARTICULAR AND LOCKING LARGE FRAGMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BIOFIRE FILMARRAY V.1.7 RESPIRATORY PANEL

    FDA Adverse Event
    Malfunction ·BIOFIRE DIAGNOSTICS, LLC·Product code QDS·December 20, 2019

    V.A.C. THERAPY

    FDA Adverse Event
    Injury ·KCI USA INC.·Product code OMP·June 19, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 2, 2013

    INFINITI VISION SYSTEM OZIL

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·December 22, 2010

    Captus 4000e Thyroid Uptake System, Model Numbers 5430-30151 and 5430-30152 - Product Usage: is intended to be used by trained nuclear Medicine Technologists or Nuclear Medicine Physicians to perform Thyroid Uptake Procedures.

    FDA Enforcement
    Class II ·Terminated·Capintec Inc·April 1, 2020