67 results · 20ms · Sources: EU EUDAMED, US FDA

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OSCAR BONE RESECTOR

FDA 510(k)
FDA Class 2 ·Orthopedic

ENT ENDOSCOPES

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

AIROCIDE TI02

FDA 510(k)
FDA Class 2 ·General Hospital

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

OT VERIO PRO METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 29, 2013

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN INC.·Product code NBW·May 10, 2011

VERTE-STACK SPINAL SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDIC INC.·Product code MQP·July 25, 2008