BEUDAMED
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    AQUILION LB TRITON V4.91

    FDA 510(k)
    FDA Class 2 ·Radiology

    SBRT Secure Arch, size M

    FDA UDI
    MACROMEDICS B.V.·08719425702605·SBRT Secure Arch, size M

    CASTROVIEJO CYCLODIALYSIS SPATULA

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896072770·CASTROVIEJO CYCLODIALYSIS SPATULA DOUBLE ENDED ...

    CASTROVIEJO CYCLODIALYSIS SPATULA

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896013438·CASTROVIEJO CYCLODIALYSIS SPATULA DOUBLE ENDED ...

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702491159·Elvarex Forte 3/Thigh High/Closed Toe, E-Versio...

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702379860·ELVAREX 1/THIGH HIGH/SLANT-OPEN TOE/TOP COMFORT...

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702271317·E3/AG/SL-CT-KC/NOP5-T-TC/BL

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K1230000·Rod Holder, Curved, 5.5 mm

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702557299·ELVAREX 3/KNEE HIGH/SLANT-OPEN TOE-ELEPHANTIASI...

    GORE EMBOLIC FILTER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DIGITAL CLINICAL THERMOMETER, MODEL BABY TEMP/WL-3305 AND BABY TEMP (+) /WL-3306

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CUSTOM CANNULA

    FDA UDI
    The Wells Johnson Company·B458201235000·Cannula, Custom, specify custom tip style, leng...

    Phadia 100

    FDA UDI
    Phadia AB·07333066000992·Phadia 100

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·March 31, 2026

    EON

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 17, 2013

    530G INSULIN PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OZO·September 26, 2014

    OLYMPUS BIOPSY FORCEPS

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code KGE·June 9, 2011

    TRUFILL DCS ORBIT DETACHABLE COIL SYSTEM

    FDA Adverse Event
    Malfunction ·CODMAN AND SHURTLEFF, INC·Product code HCG·June 15, 2017

    MAGNETOM Skyra (DE). Model Number: 10432915. 510(k) Numbers: K101347, K111242, K123510, K133435, K140253, K141977, K142515, K153343, K173592, K202014, K231560.

    FDA Recall
    Open, Classified ·Siemens Medical Solutions USA, Inc·Product code LNH·August 28, 2025

    UNKNOWN POLY

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·December 19, 2024