BEUDAMED
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    LUCENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Symmetry Tuttle (Singley)

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482052723·Symmetry® Forceps, Tuttle (Singley) Tissue, 14 in

    STIMULAN -CALCIUM SULFATE BONE VOID FILTER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DORNIER DIODE LASER FAMILY, INCLUDING MEDILAS D FIBERTOM, MEDILAS D SKINPULSE & MEDILAS D SKINPULSE S LASER SYSTEMS

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

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·April 22, 2013

    ADVANIX BILIARY STENT

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - SPENCER·Product code FGE·April 28, 2011

    RESTORE RECHARGABLE NEUROSTIMULATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·July 9, 2008

    REVITAN, PROXIMAL PART, CONICAL, UNCEMENTED, 75, TAPER 12/14

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code LZO·April 26, 2019

    REVITAN, DISTAL PART, STRAIGHT, UNCEMENTED, 18/260

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·May 6, 2019

    REVITAN, DISTAL PART, STRAIGHT, UNCEMENTED, 18/140

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·April 29, 2019

    REVITAN, DISTAL PART, STRAIGHT, UNCEMENTED, 26/260

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·April 26, 2019

    REVITAN, PROXIMAL PART, CYLINDRICAL, UNCEMENTED, 65, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·April 29, 2019

    REVITAN, DISTAL PART, CURVED, UNCEMENTED, 20/200

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code KWA·February 13, 2019

    REVITAN, DISTAL PART, STRAIGHT, UNCEMENTED, 20/140

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·August 7, 2018

    OPTAN, STEM, RIGHT, UNCEMENTED, 16, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·June 4, 2018

    REVITAN DIST. CURVED 16/200

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·October 5, 2018

    UNKNOWN REVITAN DISTAL STEM

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·April 23, 2019

    REVITAN®, DISTAL PART, CURVED, UNCEMENTED, 22/200

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·April 24, 2019

    REVITAN DISTAL STEM HIP IMPLANT

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·April 24, 2019

    REVITAN, DISTAL PART, STRAIGHT, UNCEMENTED, 16/140

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·February 4, 2019