BEUDAMED
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    FORESIGHT U120 URINE ANALYZER

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Epredia

    FDA UDI
    RICHARD-ALLAN SCIENTIFIC COMPANY·00673693222198·Tissue Marking Dyes are intended as an aid in t...

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319703359·Adson-Brown Tissue Forceps 4-3/4" (11.9cm), 9x9...

    DENTAL COMPUTED TOMOGRAPHY X-RAY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    FASTX STERNAL INTRAOSSEOUS DEVICE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·August 11, 2022

    T:SLIM X2 INSULIN PUMP WITH INTEROPERABLE TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·August 3, 2020

    T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code OZO·May 10, 2023

    VNS THERAPY PULSE

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·March 20, 2003

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·May 31, 2023

    T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code OZO·August 28, 2020

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·January 25, 2021

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·November 16, 2021

    GORE PRECLUDE DURA SUBSTITUTE

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code GXQ·May 24, 2013

    GORE PRECLUDE DURA SUBSTITUTE

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES, INC·Product code GXQ·May 24, 2013

    PIN, FIXATION, SMOOTH

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HTY·July 19, 2016

    ADULT INSPIRATORY HEATED BREATHING CIRCUIT

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·October 3, 2013

    AG GARMENTS CONDUCTIVE ELECTRODES, MODELS 100-104 SLEEVES,110-114 GLOVES,120-124 SOCKS,130-132 PANELS

    FDA 510(k)
    FDA Class 2 ·Neurology

    GORE PRECLUDE DURA SUBSTITUTE

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code GXQ·May 24, 2013

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·July 19, 2016