BEUDAMED
    21 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 ×

    MASTERSURG / EXPERTSURG

    FDA 510(k)
    FDA Class 1 ·Dental

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517565693·CoRoent Ant TLIF PEEK, 14x10x30mm 8°

    INTREPED, Intraosseous Fusion Device

    FDA UDI
    Auxano Medical LLC·00850055649422·INTREPED 08 Sizer

    PROSTHETIC SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    NOBLUS ULTRASOUND DIAGNOSTIC SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    LOGIC FEMORAL PS POR RIGHT SZ 2

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·February 10, 2025

    CER OPTION TYPE 1 TPR SLEVE -6

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·August 9, 2018

    TRIDENT PSL HA CLUSTER 54MM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·October 3, 2014

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·May 31, 2013

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·June 15, 2011

    CER OPTION TYPE 1 TPR SLEVE -6

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·August 8, 2018

    CER BIOLOXD OPTION HD 36MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·August 8, 2018

    LOGIC CR FEMORAL POR, LEFT, SZ 3.5

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·December 11, 2024

    G7 PPS LTD ACET SHELL 62H

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PBI·August 8, 2018

    G7 NEUTRAL E1 LINER 36MM H

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PBI·August 8, 2018

    S1S HIP HEAD CEMENT MOLD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWL·August 9, 2018

    S1S HIP NECK ADAPTER STD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWL·August 9, 2018

    HIP MOLD STEM W/REINF 13X145

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWL·August 9, 2018

    KIT BD MAX EXT ENTERIC BACTERIAL PANEL

    FDA Adverse Event
    Malfunction ·GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)·Product code PCH·June 21, 2022

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·April 26, 2023