BEUDAMED
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    CLEARSPEC SINGLE USE VAGINAL SPECULUM

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    GYRUS ACMI, INC

    FDA UDI
    Gyrus ACMI, LLC·00821925011601·AUSTIN STRAIGHT CHISEL 1.09 MM BLADE WIDTH STAI...

    PAL™

    FDA UDI
    Merit Medical Systems, Inc.·00884450055144·

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450185261·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694003193·Right L Plate, 12mm, Rigid

    OIC Sliding Hip Screw (SHS) System

    FDA UDI
    ORTHOPAEDIC IMPLANT COMPANY, THE·M696SHS1300460·SLIDING HIP SCREW PLATE, 130 DEGREE, 2 HOLE, ST...

    OIC Sliding Hip Screw (SHS) System

    FDA UDI
    ORTHOPAEDIC IMPLANT COMPANY, THE·10811998032433·SLIDING HIP SCREW PLATE, 130 DEGREE, 2 HOLE, ST...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197044370·Dressing Forceps Mod. USA 180mm, 7"

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197044325·Dressing Forceps Mod. USA 120mm,...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197044356·Dressing Forceps Mod. USA 145mm,...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197044387·Dressing Forceps Mod. USA 200mm, 8"

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197044332·Dressing Forceps Mod. USA 130mm,...

    M SEIRES PATIENT MONITOR MODEL M66, M69, M8000, M9000, M7000

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HOSMAN USB BLOOD PRESSURE MONITOR; WRIST TYPE AND UPPER ARM TYPE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RD SET YI

    FDA Adverse Event
    Malfunction ·MASIMO - 52 DISCOVERY·Product code DQA·March 29, 2021

    RD SET DCI

    FDA Adverse Event
    Malfunction ·MASIMO - 15750 ALTON PKWY·Product code DQA·February 10, 2023

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 27, 2025

    ACCU-CHEK ® AVIVA PLUS TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·May 24, 2013

    UNKNOWN_PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·September 30, 2014

    CORDLESS DRIVER 3

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code GET·May 5, 2011