41 results · 30ms · 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.

GRYPHON P BR DS ANCHOR W/OC

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code MAI·July 11, 2017

GRYPHON P BR DS ANCHOR W/OC

FDA Adverse Event
Injury ·DEPUY MITEK LLC US·Product code MAI·September 3, 2019

GRYPHON P BR DS ANCHOR W/OC

FDA Adverse Event
Injury ·MEDOS INTERNATIONAL SàRL·Product code MAI·September 3, 2019

GRYPHON P BR DS ANCHOR W/OC

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code MAI·November 29, 2018

GRYPHON P BR DS ANCHOR W/OC

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code MAI·October 3, 2018

GRYPHON P BR DS ANCHOR W/OC

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code MAI·July 6, 2020

M2A 38MM MOD HD -6MM NK

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KWA·October 29, 2014

MEDISENSE OPTIUM

FDA Adverse Event
Malfunction ·Product code NBW·August 12, 2011

VITALITY 2

FDA Adverse Event
Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 8, 2013

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·August 5, 2025

L3C0600 - CURE PRODUCTS

FDA Adverse Event
Malfunction ·CONVATEC INC·Product code GBM·July 19, 2022

GRYPHON P BR DS ANCHOR W/OC

FDA Adverse Event
Injury ·DEPUY MITEK LLC US·Product code MAI·March 14, 2019

GRYPHON P BR DS ANCHOR W/OC

FDA Adverse Event
Injury ·DEPUY MITEK LLC US·Product code MAI·March 14, 2019

GRYPHON BR ANCHOR W/ PROKNOT TECHNOLOGY

FDA Adverse Event
Injury ·DEPUY MITEK·Product code MAI·March 16, 2017

GRYPHON P BR DS ANCHOR W/ORTHOCORD

FDA Adverse Event
Injury ·DEPUY MITEK·Product code MAI·March 16, 2017

GRYPHON P BR DS ANCHOR W/OC

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code MAI·August 24, 2018

GRYPHON ORTHOCORD

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code MAI·April 9, 2026

GRYPHON P BR DS ANCHOR W/OC

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code MAI·January 25, 2019

GRYPHON P BR DS ANCHOR W/OC

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code MAI·January 14, 2019

GRYPHON ORTHOCORD

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code MAI·April 8, 2026