BEUDAMED
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    CRYOVALVE SG PULMONARY HUMAN HEART VALVE (AND CONDUIT)

    FDA 510(k)
    FDA Unclassified ·Unknown

    DELTA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613252600145·DELTA 10MM BURR HOLE COVERPLATE, 0.5MM

    MICASEPT OVERHOLT-GEISSENDORFER DISSECTOR

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896011014·MICASEPT OVERHOLT-GEISSENDORFER DISSECTOR WITH ...

    Cosmolock

    FDA UDI
    Kalitec Direct LLC·B07311K0120210·Assembly, Screwdriver, Extended Tab, Cannulated...

    HEMOSTATIX THERMAL SCALPEL SYSTEM - #12 BLADE

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

    VITAL SCIENTIFIC APTT, APTT & QUIKCOAG APTT

    FDA 510(k)
    FDA Class 2 ·Hematology

    EQUINOXE PRIMARY SHOULDER COMPONENTS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWS·August 25, 2022

    DURATA STS OPTIM ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL INC., CRMD·Product code NVY·January 13, 2014

    LINOX SMART SD 65/16

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code NVY·May 3, 2013

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 18, 2011

    PUMP MMT-1781KL 670G MG RPL

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·December 15, 2021

    PUMP MMT-1782K 670G V4.11 MM

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·July 19, 2021

    PUMP MMT-1781K 670G V4.11 MG

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·November 17, 2021

    SYRINGE 1.0ML 30GA 8MM 10BAG 500 L AMR

    FDA Adverse Event
    Malfunction ·EMBECTA MEDICAL I LLC - HOLDREGE, NE·Product code FMF·July 25, 2024

    TVT DISPOSABLE KIT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·April 9, 2020

    WATCHMAN FLX LAA CLOSURE DEVICE & DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NGV·January 12, 2022

    UNKNOWN IMPLANT

    FDA Adverse Event
    Injury ·NOBEL BIOCARE AB·Product code DZE·September 30, 2021

    CNS-6801A

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·August 18, 2021

    UNKNOWN IMPLANT

    FDA Adverse Event
    Injury ·NOBEL BIOCARE AB·Product code DZE·September 30, 2021

    GF-210RA

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code CCK·June 16, 2021