BEUDAMED
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    NDS THEOPHYLLINE TEST KIT & NDS TDM CALIBRATOR SET

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Master Series

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746094637·DB BRACKET MASTER SERIES MAND RIGHT CUSPID 018 ...

    ZAVATION

    FDA UDI
    Zavation LLC·00842166151031·WHITNEY 12mmx14mm , 0deg , 09mm

    Rampart One Lumbar Interbody Fusion System

    FDA UDI
    SPINEOLOGY INC.·M7404900009·Handheld Variable Angle Awl

    mahe medical GmbH

    FDA UDI
    mahe medical gmbh·04050659210301·Bone wire in coils of 10m _x000D_...

    Bone wire in coils of 10m 0.9mm

    FDA UDI
    mahe medical gmbh·EMAH00409000090·Bone wire in coils of 10m 0.9mm

    AcQMap 3D Imaging and Mapping Catheter, Model 900009

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    THD SLIDE ONE

    FDA 510(k)
    FDA Class 2 ·Radiology

    SPIRAL RADIUS RODDING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    900-009 Mittleman Geniomandibular Groove Jowl Sizer Set

    FDA UDI
    IMPLANTECH ASSOCIATES, INC.·M7249000091·Jowl Sizer Set

    MINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·May 4, 2024

    MINIMED 770G US SYSTEM BLE CONNECT 3.0 MG/DL

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·July 25, 2022

    MINIMED 770G US SYSTEM BLE CONNECT 3.0 MG/DL

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·February 9, 2023

    LONG NAIL KIT R1.5, TI, LEFT GAMMA3 10X260MM X 12

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·September 6, 2012

    Stimulator, Bone Growth, Non-Invasive

    FDA Pre-Market Approval
    FDA Class 2 ·SONIC ACCELERATED FRACTURE HEALING SYSTEM MODEL 2A

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·June 27, 2014

    CONTOUR

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE, LLC·Product code NBW·November 8, 2010

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·December 26, 2012

    Stimulator, Ultrasound And Muscle, For Use Other Than Applying Therapeutic Deep

    FDA Pre-Market Approval
    FDA Class 2 ·SONIC ACCELERATED FRACTURE HEALING SYSTEM MODEL 2000

    Stimulator, Ultrasound And Muscle, For Use Other Than Applying Therapeutic Deep

    FDA Pre-Market Approval
    FDA Class 2 ·EXOGEN ULTRASOUND BONE HEALING SYSTEM