69 results · 21ms · Sources: EU EUDAMED, US FDA

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TENS/NMES/FES STIMULATING ELECTRODE

FDA 510(k)
FDA Class 2 ·Neurology

HEALTH-PLUS, SANITEX, RELIANCE MULTIPLY POWDER FREE POLYMER AND NITRILE COATED (BLUE)

FDA 510(k)
FDA Class 1 ·General Hospital

MODIFICATION TO DEPUY C-STEM SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FCG·July 16, 2014

ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·October 25, 2018

ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·November 21, 2018

ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FCG·November 27, 2018

FCG KIT, NEEDLE, BIOPSY

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FCG·April 6, 2020

ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·January 8, 2019

ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·August 28, 2018

FCG KIT, NEEDLE, BIOPSY

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FCG·April 6, 2020

FCG KIT, NEEDLE, BIOPSY

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FCG·April 6, 2020

ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·June 28, 2019

ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FCG·April 4, 2019

ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·September 6, 2018

ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·August 1, 2019

ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FCG·July 12, 2019

M2A-MAGNUM MOD HD SZ 46MM

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KWA·April 29, 2013

PRECISION®

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·May 10, 2011

TERUMO ADVANCED PERFUSION SYSTEM 1

FDA Adverse Event
Malfunction ·TERUMP CARDIOVASCUALR SYSTEMS CORP·Product code DTQ·July 28, 2008