6,245 results · 32ms · Sources: EU EUDAMED, US FDA

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UNIDENTIFIED ASR HEAD

FDA Adverse Event
Injury ·GBR·Product code KXA·September 23, 2016

EPI-GUIDE BIORESORBABLE BARRIER MATRIX

FDA Adverse Event
Injury ·KENSEY NASH CORP.·Product code LYC·May 13, 2013

CONTACT RC INICELL

FDA Adverse Event
Injury ·THOMMEN MEDICAL AG·Product code DZE·June 6, 2022

ETIII SA

FDA Adverse Event
Injury ·HIOSSEN, INC.·Product code DZE·October 3, 2019

CYTOPLAST TI-250 TITANIUM-REINFORCED MEMBRANE

FDA Adverse Event
Injury ·OSTEOGENICS BIOMEDICAL, INC.·Product code LYC·March 7, 2013

CYTOPLAST REGENTEX TITANIUM 250

FDA Adverse Event
Injury ·OSTEOGENICS IOMEDICAL, INC.·Product code LYC·October 25, 2018

COPIOS PERICARDIUM MEMBRANE

FDA Adverse Event
Injury ·TUTOGEN MEDICAL GMBH (TMI)·Product code NPL·June 18, 2025

COPIOS PERICARDIUM MEMBRANE

FDA Adverse Event
Injury ·TUTOGEN MEDICAL GMBH (TMI)·Product code NPL·June 18, 2025

COPIOS PERICARDIUM MEMBRANE

FDA Adverse Event
Injury ·TUTOGEN MEDICAL GMBH (TMI)·Product code NPL·June 18, 2025

CYTOPLAST TITANIUM-REINFORCED PTFE MEMBRANE

FDA Adverse Event
Injury ·OSTEOGENICS BIOMEDICAL, INC.·Product code LYC·May 8, 2015

SUPERLINE

FDA Adverse Event
Injury ·DENTIUM USA·Product code DZE·November 17, 2022

MEMBRAGEL

FDA Adverse Event
Injury ·BIORA AB·Product code NPK·October 19, 2010

INTEGRA-CP

FDA Adverse Event
Injury ·BICON, LLC·Product code DZE·August 27, 2018

SURGIGUIDE - 1 IMPLANT

FDA Adverse Event
Injury ·DENTSPLY SIRONA K.K. DDSC FACTORY·Product code NDP·January 3, 2025

COBAS 8000 COBAS ISE MODULE

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·March 22, 2021

PRIMETAPER EV Ø3.6 X 11MM OS

FDA Adverse Event
Injury ·DENTSPLY IMPLANTS (A DIVISION OF DENTSPLY IH AB)·Product code DZE·May 11, 2026

CYTOPLAST TI-250 TITANIUM-REINFORCED MEMBRANE

FDA Adverse Event
Injury ·OSTEOGENICS BIOMEDICAL, INC.·Product code LYC·March 7, 2013

COBAS 8000 C 702 MODULE

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·April 19, 2021

OMNIPOD DASH¿ INSULIN MANAGEMENT SYSTEM

FDA Adverse Event
Malfunction ·INSULET CORPORATION·Product code LZG·May 13, 2020

OMNIPOD DASH¿ INSULIN MANAGEMENT SYSTEM

FDA Adverse Event
Malfunction ·INSULET CORPORATION·Product code LZG·March 17, 2020