BEUDAMED
    49 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 ×

    BUILD-IT FR

    FDA 510(k)
    FDA Class 2 ·Dental

    MTI

    FDA UDI
    Medical Technology Industries, Inc.·10840118404867·Exam Light, CLARUS 4 LED w/Floor Stand

    ACE

    FDA UDI
    ACE SURGICAL SUPPLY CO., INC.·00614950016594·CURETTE BONE LUCAS #87 D/E 7" 18CM

    NA

    FDA UDI
    DEPUY SPINE, LLC·10705034007069·SPINAL INSTRUMENT TRIAL SPACER 11 x 11 x 25mm

    SILVERVENT

    FDA UDI
    Andreas Fahl Medizintechnik-Vertrieb GmbH·04051948000269·SILVERVENT 2 IC, SIZE 11

    TruFlex™

    FDA UDI
    Ortho Organizers, Inc.·00190707125417·TRUFLEX NiTi Euro Lower 19x25 (10pk)

    TruFlex

    FDA UDI
    ORTHO TECHNOLOGY, INC.·00190730013514·NiTi Euro Lower 19x25 10 archwires per pack

    intellijoint HIP®

    FDA UDI
    Intellijoint Surgical Inc·00628184002117·Platform, Femur, G2, 11mm

    e-vive NMES System with Post-Op Brace; Large/XL, Left (2.0 Dock)

    FDA UDI
    Motive Health, Inc.·00854691008360·e-vive NMES System with Post-Op Brace; Large/XL...

    QB1 NMES System

    FDA UDI
    Motive Health, Inc.·00854691008209·QB1 NMES System with Post-Op Brace; L/XL, Left

    MODIFIED HYDROPHILIC COATED GUIDEWIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    IMMAGE IMMUNOCHEMISTRY SYSTEM LIPOPROTEIN(A) LPAX REAGENT, ARRAY SYSTEM LIPOPROTEIN(A) LPA REAGENT, LIPOPROTEIN(A) CALIB

    FDA 510(k)
    FDA Class 2 ·Immunology

    N/A

    FDA UDI
    ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024367562·Soft Felt, White

    FLOW-I C20 ANESTHESIA SYSTEM

    FDA Adverse Event
    Malfunction ·MAQUET CRITICAL CARE AB·Product code BSZ·April 10, 2025

    GYNECARE INTERGEL

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code MCN·June 29, 2004

    MAVERICK²¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LOX·March 12, 2013

    AUTOPLEX W/O NDL. INTL

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS PUERTO RICO·Product code JDZ·February 18, 2011

    OPTIVANTAGE DH

    FDA Adverse Event
    Injury ·LIEBEL-FLARSHEIM CO.·Product code IZQ·February 19, 2008

    ECHELON FLEX POWERED VASCULAR STAPLER WITH ADVANCED PLACEMENT TIP

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 1, 2021

    Impella 5.5 SmartAssist Set, JP; Product Code: 1000211;

    FDA Recall
    Open, Classified ·Abiomed, Inc.·Product code OZD·August 5, 2024