BEUDAMED
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    LYFO-KWIK OMI KIT

    FDA 510(k)
    FDA Class 1 ·Microbiology

    OMI RETRACTABLE SAFETY SYRINGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    OMI RETRACTABLE SAFTEY SYRINGE, VARIOUS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    OMI OCCIPITAL CERVICAL LOOP, MODEL A1089

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OMI

    FDA Adverse Event
    Malfunction ·OMI·Product code HBL·April 21, 1999

    OMI

    FDA Adverse Event
    Other ·OHIO MEDICAL INSTRUMENT CO.·Product code FPO·October 26, 2001

    OMI

    FDA Adverse Event
    Other ·OHIO MEDICAL INSTRUMENT CO.·Product code INW·October 23, 2002

    MAYFIELD

    FDA Adverse Event
    OHIO MEDICAL INSTRUMENT CO., INC.·Product code HBL·February 3, 2003

    VINTAGE PRO POWD OPAQ OM-Y 15

    FDA UDI
    SHOFU DENTAL CORPORATION·E235P00550·VINTAGE PRO POWD OPAQ OM-Y 15

    VINTAGE PRO PASTE OPAQ 6G OM-Y

    FDA UDI
    SHOFU DENTAL CORPORATION·E235P00250·VINTAGE PRO PASTE OPAQ 6G OM-Y

    VINTAGE PRO POWD OPAQ OM-Y 50G

    FDA UDI
    SHOFU DENTAL CORPORATION·E235P00850·VINTAGE PRO POWD OPAQ OM-Y 50G

    MAYFIELD BASE UNIT

    FDA Adverse Event
    Injury ·OHIO MEDICAL INSTRUMENT·Product code HAW·May 4, 1999

    MAYFIELD CLAMP

    FDA Adverse Event
    Malfunction ·OMI·Product code HBL·April 22, 2003

    BONART'S ARTEOTOMY OMI AND OPI ULTRASONIC SURGERY SYSTEM & ACCESSORIES

    FDA 510(k)
    FDA Class 2 ·Dental

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code NIQ·May 1, 2006

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS LLC (PR)·Product code NIQ·May 19, 2005

    OMI SURGICAL PRODUCTS

    FDA Adverse Event
    Injury ·SM USA INC·Product code HBL·May 18, 2006

    UNISTIK

    FDA Adverse Event
    Malfunction ·OWEN MUMFORD LIMITED·Product code FMK·February 7, 2024

    UNIFINE PENTIPS

    FDA Adverse Event
    Injury ·OWEN MUMFORD, LTD·Product code FMI·May 26, 2010

    SYMMETRY BYPASS SYSTEM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.·Product code FZP·October 23, 2003