BEUDAMED
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    DURAGEN DURAL GRAFT MATRIX

    FDA 510(k)
    FDA Class 2 ·Neurology

    Modulus

    FDA UDI
    Nuvasive, Inc.·00195377049902·Modulus ALIF HL Trial, 12x38x30mm 30°

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091982180·posteriors; shade A3.5 light; size M; upper jaw

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111010774·ENDOLAR SCISS LF CVD 2MM 9.75"

    ENDOPATH ENDOSCOPIC MULTIFEED STAPLER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GAG·June 23, 1998

    SPEAC System

    FDA 510(k)
    FDA Class 2 ·Neurology

    PERMA FIBER,MODEL 441; PERMA MESH, MODEL 440

    FDA 510(k)
    FDA Class 2 ·Dental

    SEE H10

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code NBC·April 18, 2013

    ADVIA CENTAUR CEA AND BR ASSAY

    FDA Adverse Event
    Other ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code DHX·June 27, 2008

    ASR ACETABULAR CUPS 58

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·February 28, 2013

    MICRO INTRODUCER, 7F 11CM

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code DYB·January 18, 2011

    DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·September 27, 2016