BEUDAMED
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    PLUG-LOK CEMENT RESTIRCTOR

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

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515206762·Boss Steinman Pin Smooth, 9", single diamond, r...

    ADAS 3D

    FDA 510(k)
    FDA Class 2 ·Radiology

    CLEARWAVE PHOTOTHERAPY SYSTEM FOR ACNE, MODEL: CWST2

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

    RIATA ST OPTIM ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·May 5, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 15, 2012

    CAPSUREFIX NOVUS

    FDA Adverse Event
    MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 10, 2010

    Promote, Sterile EO, Model #/ Part #: 3207-30/60010740-207, 60010740-407; 3207-36/60010743-207, 60010743-407; 3213-36/50022126-001, 60013879-307, 60013879-407, 60013879-707; CD3211-36/100006984,100012548, 100012550, 100016680, 100031621, 100035618, 100035619, 100042487, 100047194; CD3211-36Q/100004091, 100004093,100019784, 100035620, 100042486, 100047054; CD3215-36/100006995, 100010246, 100010247, 100010249, 100010250, 100012569, 100012570, 100034981, 100046577, 100046802, 60019065; CD3215-36Q/100004059, 100004060, 100004061, 100023304, 100030590, 100033678, 100042492, 100046803, 100046906

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018