BEUDAMED
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    Kensie

    FDA UDI
    Kenmark Optical, Inc.·00715317085588·OMG Caramel Tortoise Spectacle

    Kensie

    FDA UDI
    Kenmark Optical, Inc.·00715317085571·OMG Crystal Nude Spectacle

    Kensie

    FDA UDI
    Kenmark Optical, Inc.·00715317085472·OMG Turquoise Tort Spectacle

    Precision ™ OMG™

    FDA UDI
    BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·08714729767824·Connector-M

    Precision Spectra™ OMG

    FDA UDI
    BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·08714729861546·Adapter

    Precision ™ OMG™

    FDA UDI
    BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·08714729767817·Connector-A

    Precision ® OMG ™

    FDA UDI
    BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·M365SC93100·OMG ™ Connector-M

    Precision ® OMG ™

    FDA UDI
    BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·M365SC93050·OMG ™ Connector-A

    DA VINCI SURGICAL SYSTEM

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL,INC.·Product code NAY·July 1, 2016

    JOSTENT CORONARY STENT GRAFT

    FDA Adverse Event
    Other ·JOMED GMBH·Product code DSY·July 24, 2002

    VINTAGE PRO PASTE OPAQ 6G OM-G

    FDA UDI
    SHOFU DENTAL CORPORATION·E235P00220·VINTAGE PRO PASTE OPAQ 6G OM-G

    VINTAGE PRO POWD OPAQ OM-G 15G

    FDA UDI
    SHOFU DENTAL CORPORATION·E235P00520·VINTAGE PRO POWD OPAQ OM-G 15G

    VINTAGE PRO POWD OPAQ OM-G 50G

    FDA UDI
    SHOFU DENTAL CORPORATION·E235P00820·VINTAGE PRO POWD OPAQ OM-G 50G

    HITACHI MODULAR P

    FDA Adverse Event
    ROCHE DIAGNOSTICS·Product code JJE·September 9, 2005

    CLEAR CARE

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC. / ALCON RESEARCH, LLC·Product code LPN·December 9, 2019

    ONE TOUCH PROFILE

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·April 2, 2002

    SURESTEP

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CGA·June 1, 1999

    ONE TOUCH BASIC

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·September 23, 2002

    OMG (Observational Mechanical Gateway) Connector - A Model Number SC-9305 The Precision Spinal Cord Stimulator System is indicated as an aid in the management of chronic intractable pain of the trunk and/or limbs, including unilateral or bilateral pain associated with following: failed back surgery syndrome, intractable low back pain and leg pain. The Precision System includes an implantable l6-output, multi-channel stimulator (lPO - Implantable Pulse Generator) with a rechargeable battery power source. The lPG, commonly implanted in the abdomen or buttock area, can be configured to accept one or two leads. The leads are implanted in the epidural space, adjacent to the spinal column. The stimulation delivered at the distal end of the lead is intended to mask the pain signals.

    FDA Recall
    Terminated ·Advanced Bionics Corporation 12740 San Fernando Rd Bldgs. 1 & 3 Sylmar CA 91342·Product code LGW·April 22, 2008

    Salmonella O Group Pool OMG serum, 3 mL

    FDA UDI
    Ssi Diagnostica A/S·05713106402184·Rabbit anitserum, Ready to use