BEUDAMED
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    FEA INDUSTRIES, INC.

    FDA registration
    FEA INDUSTRIES, INC.·1 product·🇺🇸 United States

    Fysh Sunwear

    FDA UDI
    WestGroupe Optical Inc·00676190870947·Sunglasses ( tinted non-prescription spectacles )

    UNKNOWN COPELAND SHOULDER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWS·October 16, 2014

    FEA,DSCTR 5MM BLUNT NOSE

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW INC. ENDOSCOPY DIVISION·Product code GCJ·September 11, 2002

    FEA,DSCTR 5MM BLUNT NOSE

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC., ENDOSCOPY DIVISION·Product code HRX·December 21, 2001

    FEA,JAW,GRSPR.S/A ATRMTC

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC., ENDOSCOPY DIVIS·Product code KOG·September 14, 2001

    HYDRUS MICROSTENT

    FDA Adverse Event
    Injury ·IVANTIS INC·Product code OGO·April 18, 2025

    INBONE FUSION ROD

    FDA Adverse Event
    Injury ·INBONE TECHNOLOGIES·Product code HSB·January 9, 2008

    FEA,JAW,GRSPR,D/A,ARTMTC - INTERCEPTRE

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC.ENDOSCOPY DIVIS·Product code KOG·March 12, 2002

    FARAWAVE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code QZI·December 15, 2025

    REVOLUTION CT

    FDA Adverse Event
    Injury ·GE MEDICAL SYSTEMS, LLC·Product code JAK·May 6, 2019

    MODULIFT VBR SZ.M 4MM SET SCREW DRIVER

    FDA Adverse Event
    Malfunction ·AESCULAP INC·Product code HXX·March 13, 2020

    MODULIFT VBR SZ.M 4MM SET SCREW DRIVER

    FDA Adverse Event
    Malfunction ·AESCULAP INC·Product code HXX·March 13, 2020

    J001FO 1000ML JOEY FEED BAG TYPE X30

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code LZH·October 14, 2020

    J011RO JOEY ADAPUTER TYPE X30

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code LZH·November 23, 2021

    J011RO JOEY ADAPUTER TYPE X30

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code LZH·June 26, 2020

    DYNACLIP 2-LEG STAPLE

    FDA Adverse Event
    Injury ·MEDSHAPE, INC.·Product code JDR·February 9, 2024

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code DZE·March 23, 2018

    NATURAL-KNEE II SYSTEM CONGRUENT TIBIAL INSERT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code HSH·February 20, 2009

    NATURAL-KNEE II SYSTEM CONGRUENT TIBIAL INSERT

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code HSH·January 8, 2009