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    Barco, Inc

    FDA registration
    Barco, Inc·2 products·🇺🇸 United States

    Barco Inc Portland

    FDA registration
    Barco Inc Portland·1 product·🇺🇸 United States

    Barco

    FDA UDI
    Barco, Inc.·00700621719502·LCD Color Display

    Barco

    FDA UDI
    Barco, Inc.·00700621719618·LCD Color Display

    Stryker

    FDA UDI
    Barco, Inc.·00700621719564·VGA/RGB to HDMI Converter

    Stryker

    FDA UDI
    Barco, Inc.·00700621719571·3G-SDI to HDMI Converter

    Barco

    FDA UDI
    Barco, Inc.·00700621719298·LCD Color Display

    Stryker

    FDA UDI
    Barco, Inc.·00700621719533·32" 4K Surgical Display

    Stryker

    FDA UDI
    Barco, Inc.·00700621719588·DVI to HDMI Converter

    Stryker

    FDA UDI
    Barco, Inc.·00700621719557·S-Video/Composite to HDMI Converter

    BARCO INC

    FDA Adverse Event
    Malfunction ·BARCO INC·Product code FWB·December 16, 2021

    BARCO INC

    FDA Adverse Event
    Injury ·BARCO INC·Product code FWB·October 6, 2023

    Barco MDNC-3421 DISPLAY, DIAGNOSTIC RADIOLOGY

    FDA Recall
    Terminated ·Barco N.V. President Kennedypark 35 Kortrijk Belgium·Product code PGY·January 22, 2021

    Biomet Interlok 67 mm Fixed Cruciate Tibial Plate with Locking Bar; CO-CR-MO/TI 6AL 4V Alloy; Product Number/REF 141232, Biomet Orthopedics, Inc., Warsaw, IN 46582

    FDA Recall
    Terminated ·Biomet, Inc.·Product code JWH·September 18, 2007

    DAVINCI SI

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·November 12, 2024

    Surgical Display, Model No. MDSC-2224 (24 inch), Model No. MDSC-2226 (26 inch) and Model No. MDSC-2242 (42 inch)

    FDA Recall
    Terminated ·Barco Inc.·Product code KQM·May 28, 2015

    Biomet Interlok 75 MM fixed I-Beam Tibial Plate with locking bar CO-CR-MO/TI 6AL 4V ALLOY, REF 141224, Sterile, BIOMET ORTHOPEDICS, WARSAW. IN I-Beam Tibia Plates are knee joint replacement prostheses intended for application with or without bone cement.

    FDA Recall
    Terminated ·Biomet, Inc.·Product code JWH·March 3, 2011

    Biomet Interlok 67 MM fixed Cruciate Tibial Plate with locking bar CO-CR-MO/TI 6AL 4V ALLOY, REF 141232, Sterile, BIOMET ORTHOPEDICS, WARSAW. IN I-Beam Tibia Plates are knee joint replacement prostheses intended for application with or without bone cement.

    FDA Recall
    Terminated ·Biomet, Inc.·Product code JWH·March 3, 2011

    Surgical Display, Model No. MDSC-2224 (24 inch), Model No. MDSC-2226 (26 inch) and Model No. MDSC-2242 (42 inch)

    FDA Enforcement
    Class II ·Terminated·Barco Inc.·November 11, 2015

    DARCO INTERNATIONAL, INC.

    FDA registration
    DARCO INTERNATIONAL, INC.·15 products·🇺🇸 United States