BEUDAMED
    29 results · 23ms · 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 ×

    ETYMOTIC RESEARCH ER-10D OAE PROBE

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

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040013823·Zirlux 16+ A4 98.5X18

    TiWAVE L Lumbar Cage System

    FDA UDI
    Kalitec Direct LLC·B07323K0101140·Distractor, Smooth Paddle, Lordotic, 14mm

    InTess Lumbar Cage

    FDA UDI
    Kalitec Direct LLC·B07312K0101140·Distractor, Smooth Paddle, 14mm

    READERS CHOICE

    FDA UDI
    FGX INTERNATIONAL INC.·00193033243381·

    READERS CHOICE

    FDA UDI
    FGX INTERNATIONAL INC.·00193033243398·

    READERS CHOICE

    FDA UDI
    FGX INTERNATIONAL INC.·00193033243374·

    MATIRA ANTERIOR CERVICAL SYSTEM

    FDA UDI
    Kalitec Direct LLC·B07307K0111101·AWL, 10MM SPRING LOADED

    3M QUIK TEMP TEMPORIZATION MATERIAL

    FDA 510(k)
    FDA Class 2 ·Dental

    ACUVUE 2 BRAND (ETAFILCON A) CONTACT LENS, WITH UV BLOCKER TINTED (TO MASK OR ENHANCE THE NATURAL IRIS COLOR)

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    AUTOSOFT 30

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·June 17, 2025

    AUTOSOFT 30

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·June 17, 2025

    AUTOSOFT 30

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·June 17, 2025

    NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·March 7, 2012

    MOTO PARTIAL KNEE 02.18.002LM ANATOMICAL FEMORAL COMPONENT CEMENTED S2 LM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code HSX·March 14, 2024

    ENDOTRACH TUBE 8229970 5PK 7MM EMG FLEX

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC.·Product code ETN·March 14, 2013

    SYNERGY

    FDA Adverse Event
    Injury ·SMITH AND NEPHEW, INC·Product code LPH·March 8, 2011

    VERITY DR

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

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·September 4, 2015

    ON-Q PUMP 270ML, 4ML/HR (2+2 DUALSITE SILVERSOAKER

    FDA Adverse Event
    Injury ·I-FLOW, LLC·Product code BSO·July 7, 2014