BEUDAMED
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    SLT SELECT FIBER DELIVERY SYSTEM AND CONTACT TIPS

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

    DeltaForm HD

    FDA UDI
    Merz Dental GmbH·D7091980156·DeltaForm HD upper posteriors, S, D4 -MADE IN G...

    OSSEOSPEED TM PROFILE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    SP-Fix® Spinous Process Fixation Plate, RELIEVE® Laminoplasty Fixation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·February 27, 2013

    7700

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·January 24, 2011

    OT ULTRAMINI METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 5, 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