BEUDAMED
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    FDA 510(k)
    FDA Class 2 ·Dental

    DeltaForm HD

    FDA UDI
    Merz Dental GmbH·D7091980195·DeltaForm HD lower posteriors, M, BL4 -MADE IN ...

    ZMR®

    FDA UDI
    Zimmer, Inc.·00889024364714·

    ZMR®

    FDA UDI
    Zimmer, Inc.·00889024364738·

    ZMR®

    FDA UDI
    Zimmer, Inc.·00889024364707·

    ZMR®

    FDA UDI
    Zimmer, Inc.·00889024364721·

    ENDOPATH ENDOSCOPIC MULTIFEED STAPLER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GAG·January 14, 1998

    Frigitronics adapter

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    NACERA Z AND NACERA Z MEDIUM

    FDA 510(k)
    FDA Class 2 ·Dental

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·00842962154427·SMITH PETERSON RACK, 13"X12"X1 7/8", HOLDS NINE...

    ANIMAS INSULIN CARTRIDGE

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·February 27, 2013

    NEXGEN LCCK ARTICULAR SURFACE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·February 1, 2011

    HALOFLEX (115V) GENERATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code GEI·July 2, 2014

    1.85MM TI MATRIX SCREW SELF-TAPPING/4MM

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code JEY·January 21, 2015

    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