34 results · 30ms · Sources: EU EUDAMED, US FDA

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ACCIN UNI-KNEE SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

DISETRONIC PENFINE INSULIN INJECTION PEN NEEDLE

FDA 510(k)
FDA Class 2 ·General Hospital

CONSTELLATION CATHETER, MODEL 8031

FDA 510(k)
FDA Class 2 ·Cardiovascular

RESONANCE STENT SET

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FAD·December 13, 2018

BD PHOENIX¿ NMIC-311

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 19, 2026

BD PHOENIX¿ NMIC-311

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 19, 2026

RESONANCE STENT SET

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FAD·October 31, 2018

AED PRO

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·March 28, 2013

ACCU-CHEK COMPACT TEST DRUM

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·June 19, 2008

SYNCHROMED

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·April 15, 2011

RESONANCE STENT SET

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FAD·October 6, 2023

RESONANCE STENT SET

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FAD·July 25, 2018

RESONANCE STENT SET

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FAD·May 29, 2015

BD PHOENIX¿ NMIC/ID-307

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·September 23, 2025

BD PHOENIX¿ NMIC-311

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·December 18, 2025

BD PHOENIX¿ NMIC-311

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·August 7, 2025

BD PHOENIX¿ NMIC-311

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·August 7, 2025

BD PHOENIX¿ NMIC-311

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·August 7, 2025

BD PHOENIX¿ NMIC-311

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·August 7, 2025

BD PHOENIX¿ NMIC-311

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·August 7, 2025