BEUDAMED
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    MODIFICATION TO PROWESS PRO-SIM

    FDA 510(k)
    FDA Class 2 ·Radiology

    NA

    FDA UDI
    Synthes GmbH·10886982201393·REDUCTION FORCEPS WITH POINTS BROAD-RATCHET

    Polystar HK

    FDA UDI
    Merz Dental GmbH·D7091984196·anteriors; shade A4; mould D 68

    P.F.C.

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295252535·P.F.C. TIBIAL INSERT FIXED BEARING CURVED 6 10m...

    PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SURGICAL INSTRUMENTS (VARIOUS TYPES & SIZES)

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·February 28, 2013

    VIRTUOSO DR

    FDA Adverse Event
    Death ·MEDTRONIC MED REL, INC.·Product code LWS·February 10, 2011

    MODULAR HANDLE

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LXH·August 6, 2014

    Angiotech Pediatric Bone Marrow Needle. Pediatric Bone Marrow Needle. STERILE. Product Number: ION18015. 510k K980196. MEDICAL DEVICE TECHNOLOGIES, INC. 3600 Southwest 74th Avenue, Gainesville, Florida 32608 U.S.A. Intended Use: Pediatric Bone Marrow Needle

    FDA Recall
    Terminated ·Medical Device Technologies, Inc.·Product code KNW·September 1, 2009