BEUDAMED
    23 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 ×

    CLEAR GUIDE ONE

    FDA 510(k)
    FDA Class 2 ·Radiology

    3M™ Unitek™

    FDA UDI
    3M UNITEK CORPORATION·00652221038036·Unitek(TM) Bicuspid Band General Purpose Wide L...

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B167311418060·

    TALOS® HA PEEK IBF

    FDA UDI
    MEDITECH SPINE, LLC·B167321418060·

    ZAVATION

    FDA UDI
    Zavation LLC·00842166186682·14mm X 18mm 6° Trial

    Monterey™ AL

    FDA UDI
    VB Spine LLC·10888857586970·M/L AL Implant Inserter 18/20 mm

    PASSING NEEDLE WITH ETHIBOND, PANACRYL OR ORTHOCORD SUTURE; AND PASSING NEEDLE WITH ETHIBOND LOOP

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    AIDERA DIASEND SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SiNAPTIC Osteotomy Wedge System

    FDA UDI
    SINTX Technologies, Inc.·G817S111141806·Cotton Wedge, 14W x 18D x 6H

    SiNAPTIC Osteotomy Wedge System

    FDA UDI
    SINTX Technologies, Inc.·G81711325141806·Osteotomy Wedge System, Cotton Trial 14W x 18D ...

    VDW GOLD/SILVER CONTRA ANGLE

    FDA Adverse Event
    Malfunction ·DENTSPLY VDW GMBH·Product code EGS·December 24, 2020

    ADVANTA 2 FRAME

    FDA Adverse Event
    Malfunction ·HILL-ROM MEXICO·Product code FNL·August 20, 2021

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 28, 2013

    R3

    FDA Adverse Event
    Injury ·SMITH AND NEPHEW, INC.·Product code LXH·June 27, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 4, 2014

    POLARIS SCREW, DIA. 6.5 X UNKNOWN LENGTH

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE, INC.·Product code NKB·May 28, 2025

    POLARIS SCREW, DIA. 6.5 X UNKNOWN LENGTH

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE, INC.·Product code NKB·May 28, 2025

    POLARIS SCREW, DIA. 6.5 X UNKNOWN LENGTH

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE, INC.·Product code NKB·May 28, 2025

    POLARIS SCREW, DIA. 6.5 X UNKNOWN LENGTH

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE, INC.·Product code NKB·May 28, 2025

    ARCTIC SUN 5000

    FDA Adverse Event
    Malfunction ·MEDIVANCE, INC. ¿ 1725056·Product code DWJ·June 10, 2019