BEUDAMED
    50 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 ×

    LEGION Porous CR Narrow Femoral Components

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VEO® Lateral Interbody Fusion System

    FDA UDI
    Choice Spine, LP·00840996133661·LATERAL,RADIAL CLAMP,16 HOLE

    VIBERECT PENILE VIBRATORY STIMULATION DEVICE

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    COLLEAGUE VOLUMETRIC INFUSION PUMP

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ALINITY I TOXO IGG REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code LGD·March 31, 2026

    ARCHITECT TOXO IGG

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code LGD·April 27, 2026

    ARCHITECT TOXO IGG

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code LGD·March 19, 2026

    PFC SIGMA TIB TRAY CEM SZ3

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·October 22, 2008

    ACRYSOF

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·August 10, 2011

    UNIFY ASSURA CRT-D

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·July 8, 2013

    ALINITY I TOXO IGG REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code LGD·April 8, 2026

    ALINITY I TOXO IGG REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code LGD·March 4, 2026

    LOCKING SCREW, FULLY THREADED 5X45 MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·October 30, 2009

    ALINITY I TOXO IGG REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code LGD·April 2, 2026

    Ultra-Drive Irrigation Tubing Assembly, Reference Number 423834 - Product Usage: Item used with the UltraDrive System to provide proper irrigation during the cutting and removal of bone and acrylic bone cement in orthopedic applications.

    FDA Enforcement
    Class II ·Terminated·Zimmer Biomet, Inc.·July 24, 2019

    ARCHITECT TOXO IGG

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code LGD·July 31, 2025

    ARCHITECT TOXO IGG

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code LGD·November 10, 2025

    ALINITY I TOXO IGG

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code LGD·July 14, 2025

    ALINITY I TOXO IGG REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code LGD·March 18, 2025

    ALINITY I TOXO IGG REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code LGD·March 13, 2026