42 results · 28ms · Sources: EU EUDAMED, US FDA

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STINGRAY GUIDEWIRES

FDA 510(k)
FDA Class 2 ·Cardiovascular

ArgenZ HT+ 95x25 B1

FDA UDI
ARGEN CORPORATION, THE·D818122795·Dental porcelain/ceramic restoration kit

MODIFICATION TO THE MAESTRO SYSTEM

FDA 510(k)
FDA Class 2 ·Dental

SIGNATURE PLANNER; SIGNATURE GUIDES

FDA 510(k)
FDA Class 2 ·Orthopedic

PROFEMUR(R) Z STEM

FDA Adverse Event
Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LPH·May 21, 2013

UNKNOWN DEPUY HEAD

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWY·June 3, 2011

FREESTYLE FREEDOM

FDA Adverse Event
Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·August 13, 2008

CXI SUPPORT CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KRA·May 12, 2017

CXI SUPPORT CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KRA·August 25, 2017

AGC DA2000 KN TIB BRG 71/75X8

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code NRA·April 9, 2026

CXI SUPPORT CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KRA·August 8, 2017

CXI SUPPORT CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KRA·March 7, 2017

CXI SUPPORT CATHETER

FDA Adverse Event
Injury ·COOK INC·Product code KRA·August 27, 2020

CXI SUPPORT CATHETER

FDA Adverse Event
Injury ·COOK INC·Product code KRA·April 24, 2019

CXI SUPPORT CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KRA·April 18, 2019

CXI SUPPORT CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KRA·July 25, 2018

CXI SUPPORT CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KRA·April 12, 2017

CXI SUPPORT CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KRA·January 15, 2020

CXI SUPPORT CATHETER

FDA Adverse Event
Injury ·COOK INC·Product code KRA·February 17, 2020

VANGUARD ROCC POR FEM S55 R

FDA Adverse Event
Malfunction ·BIOMET UK LTD.·Product code MBH·January 22, 2026