BEUDAMED
    57 results · 28ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    Dual Cure Resin Cement

    FDA 510(k)
    FDA Class 2 ·Dental

    DJO SURGICAL

    FDA UDI
    DJO, LLC·00190446887584·SPECIAL, RSP HALF MOON GLENOID REAMER RIM PLANER

    HHM

    FDA UDI
    Oticon A/S·05707131355225·G300 SC, MINIRITE 312 2.4G C045 HHM

    NA

    FDA UDI
    Synthes GmbH·10886982142887·2.4MM CORTEX SCREW SLF-TPNG WITH T8 STARDRIVE R...

    Blade Handle

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112397·BARD-PARKER HANDLE #9

    Lotion/Gel Warmer

    FDA UDI
    COMPASS HEALTH BRANDS CORP.·00853904006094·White 3 Bottle Warmer (120V)

    Diamond Orthopedic, LLC

    FDA UDI
    DIAMOND ORTHOPEDIC, LLC·B551DMD2017900·2.4mm, Cortex Screw, T8 Stardrive®, Self-Tappin...

    Medical Facets NC

    FDA UDI
    MEDICAL FACETS NC LLC·M933MDF2017900·2.4mm Cortex Screw, T8 Stardrive, Self-Tapping,...

    LnK Spinal Fixation System, OpenLoc-L Spinal Fixation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    QUANTUM SPINAL SYSTEM, QUANTUM MIS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BD 20ML ENTERAL SYRINGE, BULK NON-STERILE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code KNT·July 31, 2017

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 12, 2024

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 29, 2025

    MATRIX2 ULTRASOFT 360 SR COIL

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORP., NEUROVASCULAR DIVISION·Product code HCG·October 15, 2008

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·August 11, 2011

    INFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·July 2, 2013

    RAD-G

    FDA Adverse Event
    Malfunction ·MASIMO - 15750 ALTON PKWY·Product code DQA·October 17, 2024

    COREVALVE REVALVING SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·August 22, 2017

    GUIDE CATHETER

    FDA Adverse Event
    Injury ·CODMAN AND SHURTLEFF, INC·Product code DQY·July 30, 2020

    GUIDE CATHETER

    FDA Adverse Event
    Injury ·CODMAN AND SHURTLEFF, INC·Product code DQY·July 30, 2020