BEUDAMED
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    PHILIPS M3001A MULTI MEASUREMENT SERVER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Closed Wound Suction

    FDA UDI
    C. R. Bard, Inc.·00801741050275·ReliaVac 100 Closed Wound Suction (CWS) Kit, 7m...

    OIC Intramedullary Nail System

    FDA UDI
    ORTHOPAEDIC IMPLANT COMPANY, THE·M696TIB0903600·TIBIAL NAIL 9MM X 360MM

    OIC Intramedullary Nail System

    FDA UDI
    ORTHOPAEDIC IMPLANT COMPANY, THE·10811998037384·TIBIAL NAIL 9MM X 360MM

    CT/MR Ring & Tandem Set, 26mm, 60ø, Nucletron

    FDA UDI
    MICK RADIO NUCLEAR INSTRUMENT, INC·00817330022615·

    CT/MR R&T Ring Tube, 60ø, 26mm ring only,Nucletron

    FDA UDI
    MICK RADIO NUCLEAR INSTRUMENT, INC·00817330022622·

    ABR-2000

    FDA 510(k)
    FDA Class 2 ·Neurology

    RX G-UNIVERSAL

    FDA 510(k)
    FDA Class 2 ·Dental

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code KWP·November 15, 2013

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·April 17, 2025

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK USA, INC.·Product code KWP·October 30, 2019

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·June 26, 2020

    LOGIC FEMORAL PS CEM LEFT SZ 2.5

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·December 27, 2024

    CD HORIZON® SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·April 30, 2018

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·January 14, 2020

    CD HORIZON® SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·April 30, 2018

    RESTORE SENSOR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·May 2, 2013

    5MM PEEK MULTIFUNCTION HANDLE

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY-SAN JOSE·Product code KOG·September 15, 2014

    HOMECHOICE LOW RECIRCULATION VOLUME APD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·May 16, 2011

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 22, 2024