411 results · 24ms · Sources: EU EUDAMED, US FDA

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C-CURVE Interbody Fusion Device

FDA 510(k)
FDA Class 2 ·Orthopedic

BCI

FDA UDI
ICU MEDICAL, INC.·10610586040689·

R & D 4K RETIC

FDA 510(k)
FDA Class 2 ·Hematology

MIPAL

FDA 510(k)
FDA Class 2 ·Cardiovascular

ECHOTIP ULTRA ENDOBRONCHIAL HD ULTRASOUND NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·August 26, 2022

ECHOTIP PROCORE ENDOBRONCHIAL HD BIOPSY NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·January 16, 2024

ECHOTIP PROCORE HIGH DEFINITION ULTRASOUND BIOPSY NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·July 19, 2023

ECHOTIP ULTRA ENDOBRONCHIAL HD ULTRASOUND NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·July 26, 2022

ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·June 29, 2023

ECHOTIP PROCORE ENDOBRONCHIAL HD BIOPSY NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·March 14, 2024

ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·February 5, 2023

ECHOTIP PROCORE HIGH DEFINITION ULTRASOUND BIOPSY NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·April 9, 2024

ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·February 7, 2023

ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·June 22, 2023

ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·May 19, 2023

ECHOTIP PROCORE ENDOBRONCHIAL HD BIOPSY NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·June 7, 2023

ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·April 17, 2023

ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FCG·October 3, 2022

SCREWS

FDA Adverse Event
Injury ·SYNTHES USA·Product code HWC·October 29, 2014

ASR UNI FEMORAL IMPL SIZE 47

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·August 9, 2011