1,261 results · 21ms · 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.

ONYX

FDA Adverse Event
Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·August 14, 2023

PIPELINE

FDA Adverse Event
Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·February 8, 2023

ONYX

FDA Adverse Event
Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·February 8, 2023

PIPELINE

FDA Adverse Event
Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·February 8, 2023

VIPER 2 SCREW

FDA Adverse Event
Injury ·DEPUY SYNTHES SPINE·Product code MRW·May 15, 2017

UNKNOWN EVD CATHETER

FDA Adverse Event
Injury ·MEDTRONIC NEUROSURGERY·Product code JXG·October 21, 2016

ONYX

FDA Adverse Event
Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·July 19, 2023

ECHELON

FDA Adverse Event
Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·September 16, 2025

ONYX

FDA Adverse Event
Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·July 19, 2023

ONYX AVM

FDA Adverse Event
Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·July 24, 2025

ECHELON

FDA Adverse Event
Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·September 16, 2025

SOLITAIRE

FDA Adverse Event
Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code NRY·February 8, 2023

ONYX

FDA Adverse Event
Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·February 8, 2023

UNKNOWN SOLITAIRE

FDA Adverse Event
Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code NRY·December 23, 2024

MARATHON

FDA Adverse Event
Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·November 14, 2023

ECHELON

FDA Adverse Event
Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·November 14, 2023

PLATE, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES USA·Product code HRS·February 8, 2016

UNKNOWN SOLITAIRE

FDA Adverse Event
Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code NRY·December 23, 2024

Esophageal Protection Device For Use In Percutaneous Cardiac Catheter Ablation Procedures, Mechanical Deviation

FDA classification
FDA Class 2 ·Esophageal Protection Device For Use In Percutaneous Cardiac Catheter Ablation Procedures, Mechanical Deviation

QX World Ltd.

Manufacturer
🇭🇺 Hungary