BEUDAMED
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    VENTRIO HERNIA PATCH

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

    GYRUS ENT COGENT 2/G2 SYSTEM (GENERATOR,ACCESSORIES SOMNOPLASTY ELECTRODES AND PLASMACISION ELECTRODES)

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

    MODEL CGS TILT SEATING SYSTEM FOR POWER WHEELCHAIRS

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    IPC® STYLUS TRANSNASAL BUR

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ERL·February 6, 2015

    IPC® HANDPIECE - XPS® STRAIGHTSHOT® M4

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC·Product code ERL·June 19, 2015

    XPS® BUR

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code EQJ·September 8, 2017

    ACCY EF201 IPC FOOT CONTROL ROHS

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code HBE·September 9, 2014

    XPS® BUR - UNKNOWN

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC.·Product code EQJ·June 17, 2016

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·April 29, 2013

    SECURE 2 MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·April 13, 2011

    SETROX S 53

    FDA Adverse Event
    Injury ·BIOTRONIK GMBH AND CO.·Product code DTB·July 23, 2008

    XOM UNKNOWN ENDO

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC.·Product code EQJ·May 8, 2015

    XPS® HANDPIECE - UNKNOWN

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code HBE·November 8, 2016

    IPC® FOOTPEDAL

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ERL·March 1, 2016

    XPS® HANDPIECE - UNKNOWN

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code HBE·October 17, 2017

    INDIGO¿ DRILL

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code HBE·February 9, 2015

    GAM Kirschner Wire, Sterile R, T2 K-Wire, Sterile R and T2 K-Wire Recon, Stryker Trauma GmbH, Prof.-Kuntscher-Strasse 1-5, Schonkirchen, Germany 24232; T2 K-Wire, Sterile R Intended for the temporary stabilization of bone segments or fragments

    FDA Enforcement
    Class II ·Terminated·Stryker Howmedica Osteonics Corp.·December 28, 2016

    IPC® HANDPIECE - XPS® STRAIGHTSHOT® M5

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ERL·August 12, 2024

    INDIGO¿ BUR - ZEPPELIN - REUSABLE

    FDA Adverse Event
    Malfunction ·MDT POWERED SURGICAL SOLUTIONS·Product code ERL·September 23, 2022

    DRILL 3334800 VISAO 80K HANDPIECE

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC.·Product code ERL·July 3, 2013