50 results · 24ms · Sources: EU EUDAMED, US FDA

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SAC2 - Electrode Cream

FDA 510(k)
FDA Class 2 ·Neurology

AVS ANCHOR-C CERVICAL CAGE SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

ACTIVATOR V-E

FDA 510(k)
FDA Unclassified ·Unknown

ACDF STAND ALONE CERVICAL

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code OVE·October 8, 2025

ACDF STAND ALONE CERVICAL

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code OVE·April 25, 2025

ACDF STAND ALONE CERVICAL

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code OVE·December 22, 2025

TALENT ABDOMINAL STENT GRAFT SYSTEM

FDA Adverse Event
Death ·MEDTRONIC CARDIOVASCULAR·Product code MIH·October 8, 2008

SMALL BATTERY DRIVE

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code HWE·June 27, 2013

D-DIMER

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code GHH·August 5, 2011

ACDF 03.18.118 MECTA-C SA TIPEEK CAGE 18X15X6X7°

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code OVE·May 12, 2023

CMK OC - RASP S303

FDA Adverse Event
Malfunction ·BIOMET UK LTD.·Product code LZO·January 28, 2026

CMK OC - RASP S303

FDA Adverse Event
Malfunction ·BIOMET UK LTD.·Product code LZO·January 28, 2026

CMK OC - RASP S202

FDA Adverse Event
Malfunction ·BIOMET UK LTD.·Product code LZO·February 5, 2026

CMK OC - RASP S302

FDA Adverse Event
Malfunction ·BIOMET UK LTD.·Product code LZO·February 5, 2026

CMK OC - RASP S303

FDA Adverse Event
Malfunction ·BIOMET UK LTD.·Product code LZO·January 28, 2026

CMK OC - RASP S302

FDA Adverse Event
Malfunction ·BIOMET UK LTD.·Product code LZO·February 5, 2026

CMK OC - RASP S401

FDA Adverse Event
Malfunction ·BIOMET UK LTD.·Product code LZO·February 5, 2026

CMK OC - RASP S303

FDA Adverse Event
Malfunction ·BIOMET UK LTD.·Product code LZO·January 28, 2026

CMK OC - RASP S304

FDA Adverse Event
Malfunction ·BIOMET UK LTD.·Product code LZO·February 5, 2026

CMK OC - RASP S302

FDA Adverse Event
Malfunction ·BIOMET UK LTD.·Product code LZO·February 5, 2026