BEUDAMED
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    MODIFICATION TO CAVERMAP SURGICAL AID

    FDA 510(k)
    FDA Class 1 ·Gastroenterology, Urology

    Capstone Control Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169674806·SPACER 4031527 CONTROL 24 DEG 15X27

    Capstone Control PTC Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169677838·SPACER 5031527 CONTROL PTC 24 DEG 15X27

    Arlington PLIF Cage

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215026349·

    Verteloc Lumbar Cage

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215129392·

    FOTONA FIDELIS ER: YAG LASER SYSTEM AND ACCESORIES

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

    PRAXSYS RELIA TSH TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    AFX

    FDA Adverse Event
    Injury ·ENDOLOGIX INC.·Product code MIH·April 19, 2018

    AFX

    FDA Adverse Event
    Injury ·ENDOLOGIX INC.·Product code MIH·April 4, 2018

    AFX

    FDA Adverse Event
    Injury ·ENDOLOGIX·Product code MIH·March 31, 2020

    2031527-2012-00113

    FDA Adverse Event
    Death ·ENDOLOGIX, INC.·December 5, 2012

    2031527-2012-00115

    FDA Adverse Event
    Injury ·ENDOLOGIX, INC.·November 21, 2012

    2031527-2012-00119

    FDA Adverse Event
    Injury ·ENDOLOGIX, INC.·October 30, 2012

    2031527-2012-00118

    FDA Adverse Event
    Injury ·ENDOLOGIX, INC.·December 14, 2012

    2031527-2012-00122

    FDA Adverse Event
    Injury ·ENDOLOGIX, INC.·November 8, 2012

    2031527-2012-00120

    FDA Adverse Event
    Injury ·ENDOLOGIX, INC.·November 21, 2012

    2031527-2012-00112

    FDA Adverse Event
    Injury ·ENDOLOGIX, INC.·December 14, 2012

    2031527-2012-00108

    FDA Adverse Event
    Malfunction ·ENDOLOGIX, INC.·October 29, 2012

    2031527-2012-00133

    FDA Adverse Event
    Death ·ENDOLOGIX, INC.·December 5, 2012

    2031527-2012-00094

    FDA Adverse Event
    Injury ·ENDOLOGIX, INC.·August 15, 2012