BEUDAMED
    24 results · 31ms · 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 ×

    T2 FEMORAL NAIL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ROLLO 108X23X16E*31*MORTARA.

    FDA UDI
    AB MEDICA GROUP, S.A.·08428763004493·

    ACUFEX

    FDA UDI
    Smith & Nephew, Inc.·03596010022066·ROTARY SCISSORS 20 DEGREE HOOKED ...

    EsFlow A1 Syringe

    FDA UDI
    Spident Co., Ltd.·08809262954715·Nano-hybrid Flowable composite resin for poster...

    LightScalpel

    FDA UDI
    Lightscalpel, LLC·00851842007166·Accessory Brush, LS Handpieces

    JOBST Custom Seamless Soft

    FDA UDI
    BSN-Jobst GmbH·04059993136841·CUSTOM SEAMLESS SOFT 3/PANTY/CLOSED TOE/FOR MAN...

    JOBST Custom Seamless Soft

    FDA UDI
    BSN-Jobst GmbH·04059993141074·CUSTOM SEAMLESS SOFT 2/PANTY/CLOSED TOE/FOR MAN...

    Phonak

    FDA UDI
    Phonak AG·07613275257821·Phonak Audéo V70-10 (beige)

    4 ML LITHIUM HEPARIN SEPARATOR VACUETTE TOTAL CALCIUM

    FDA Adverse Event
    Malfunction ·GREINER BIO-ONE·Product code JKA·May 6, 2008

    STEATHSTATION TREATMENT GUIDANCE PLATFORM

    FDA 510(k)
    FDA Class 2 ·Neurology

    PC COATED FLUOROPLASTIC VENT TUBES

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    BD PHASEAL OPTIMA PROTECTOR (P20-O)

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code ONB·July 8, 2021

    CORAIL2 STD SIZE 12

    FDA Adverse Event
    Injury ·DEPUY FRANCE·Product code MEH·March 19, 2013

    V.A.C. THERAPY SYSTEM

    FDA Adverse Event
    Injury ·KCI USA, INC.·Product code OMP·March 2, 2011

    RIATA ACTIVE FIXATION LEAD

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·March 10, 2008

    BD PHASEAL OPTIMA PROTECTOR (P20-O MULTI)

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code ONB·July 8, 2021

    BD PHASEAL OPTIMA INJECTOR (N40-O MULTI)

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code ONB·July 8, 2021

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·June 2, 2025

    MAGNETOM Verio Dot. Model Number: 10684333.

    FDA Enforcement
    Class I ·Ongoing·Siemens Medical Solutions USA, Inc·October 8, 2025

    Spectral CT 7500, Software Version 5.0.0.X. Computed Tomography X-Ray System.

    FDA Enforcement
    Class II ·Ongoing·Philips North America Llc·January 24, 2024