BEUDAMED
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    ENK FIBEROPTIC ATOMIZER SET

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    NUVASIVE, INC.

    FDA registration
    NUVASIVE, INC.·60 products·🇺🇸 United States

    STIMULATION?DISSECTION INSTRUMENTS

    FDA Adverse Event
    Malfunction ·NUVASIVE, INCORPORATED·Product code ETN·October 25, 2022

    APPLIANCE, FIXATION, SPINAL INTERLAMINAL

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·October 25, 2017

    REBAR MICRO CATHETER: REBAR-18 [2.3F], 110 CM, 130 CM, 153 CM, SINGLE MARKER BAND AND 153 CM, DUAL MARKER BAND

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    APATIGHT-TCP BONE GRAFT SUBSTITUTE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SPHEREXII MAS DEFORMIT SYSTEM

    FDA Adverse Event
    Malfunction ·NUVASIVE, INC.·Product code NKB·August 20, 2013

    X-CORE 2 TI CORE, Ø18MM 28-41MM AUTOLOCK

    FDA Adverse Event
    Injury ·NUVASIVE, INC.·Product code MQP·April 16, 2024

    RELINE

    FDA Adverse Event
    Malfunction ·NUVASIVE, INC.·Product code LXH·April 25, 2024

    SIMPLIFY® CERVICAL ARTIFICIAL DISC

    FDA Adverse Event
    Injury ·NUVASIVE, INC.·Product code MJO·January 26, 2022

    SIMPLIFY® CERVICAL ARTIFICIAL DISC

    FDA Adverse Event
    Injury ·NUVASIVE, INC.·Product code MJO·January 26, 2022

    NUVASIVE® VUEPOINT® II OCT SYSTEM

    FDA Adverse Event
    Injury ·NUVASIVE INC.·Product code NKG·May 21, 2019

    SIMPLIFY® CERVICAL ARTIFICIAL DISC

    FDA Adverse Event
    Injury ·NUVASIVE, INC.·Product code MJO·January 26, 2022

    NUVASIVE® COROENT® THORACOLUMBAR SYSTEM

    FDA Adverse Event
    Malfunction ·NUVASIVE, INC.·Product code MAX·May 29, 2018

    UNKNOWN SCREW

    FDA Adverse Event
    Injury ·NUVASIVE INC·Product code NKB·March 15, 2023

    NUVASIVE EXTREME LATERAL LUMBAR IMPLANT INSERTER

    FDA Adverse Event
    Malfunction ·NUVASIVE, INC.·Product code MAX·January 6, 2023

    NUVASIVE RELINE SYSTEM

    FDA Adverse Event
    Injury ·NUVASIVE·Product code NKB·November 16, 2018

    TSRH SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·August 3, 2020

    NUVASIVE® RELINE® SYSTEM

    FDA Adverse Event
    Injury ·NUVASIVE, INC.·Product code NKB·May 3, 2018

    TSRH SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·May 11, 2020