BEUDAMED
    24 results · 24ms · 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 ×

    PRISMAFLO

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ACRYDERM SILVER ANTIMICROBIAL STRANDS MODEL A-020103

    FDA 510(k)
    FDA Unclassified ·Unknown

    O-Cryl Self Curing Acrylic Shade White X 1 lb

    FDA UDI
    PRODUCTORA Y COMERCIALIZADORA ODONTOLOGICA NEW STETIC S A·07701126626336·O-Cryl Self Curing Acrylic Shade White X 1 lb

    PureSkin

    FDA UDI
    PURELIFE, LLC·D79010201031·PureSkin Latex Powder-Free, Medium, Fully-textu...

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·H65820201031·Channels K-Files 25mm

    Channels

    FDA UDI
    HENRY SCHEIN, INC.·10304040039196·Channels K-Files 25mm, #60

    Midway Select

    FDA UDI
    MIDWAY DENTAL SUPPLY, LLC·10843717101052·Burs Finishing FG 7901, Pkg/5

    LOCATOR F-Tx

    FDA UDI
    Zest Anchors, LLC·00840481114342·LOCATOR F-Tx Abutment for 4.5 Internal Hex Conn...

    PATIENT-FITTED TMJ RIGHT FOSSA COMPONENT

    FDA Adverse Event
    Injury ·TMJ SOLUTIONS, INC.·Product code LZD·December 9, 2020

    SIMPLICITY SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AVL OPTI R ANALYZER

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    UNKNOWN LINER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·February 10, 2015

    FREESTYLE

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC.·Product code LFR·May 25, 2007

    MINICAP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·March 25, 2013

    ADVANCE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·March 10, 2011

    ACRYSOF

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·March 25, 2010

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·March 24, 2020

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·April 10, 2023

    POLARIS (TM) LOOP US W/O SHAFT HOLES

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FAD·May 7, 2026

    NRG RF TRANSSEPTAL KIT

    FDA Adverse Event
    Injury ·BAYLIS MEDICALE CIE INC·Product code DXF·December 17, 2024