41 results · 18ms · Sources: EU EUDAMED, US FDA

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AL ASKARI PERCUTANEOUS ACCESS NEEDLE HOLDER

FDA 510(k)
FDA Class 1 ·Gastroenterology, Urology

KMEDIC

FDA UDI
TELEFLEX INCORPORATED·24026704282986·RETRACTOR MEYERDING MEDIUM 25 MILLIMETER X 70 ...

NAR Kit

FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209101719·KIT, TACTICAL CRICKIT - CUSTOM

CUSA® Clarity Ultrasonic Surgical Aspirator System

FDA 510(k)
FDA Unclassified ·Unknown

GENEROS SB SMALL BONE DISTRACTION IMPLANT

FDA 510(k)
FDA Class 2 ·Orthopedic

ZIMMON BILIARY STENT SET

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

ZIMMON BILIARY STENT

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FGE·August 14, 2018

ZIMMON BILIARY STENT SET

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FGE·January 9, 2019

ZILVER 635 BILIARY SELF EXPANDING METAL STENT

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FGE·October 22, 2021

ZIMMON BILIARY STENT

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FGE·December 11, 2018

OASIS ONE ACTION STENT INTRODUCTION SYSTEM

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FGE·December 11, 2018

COTTON-LEUNG BILIARY STENT

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FGE·September 4, 2020

COTTON-LEUNG BILIARY STENT

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FGE·September 4, 2020

COTTON-LEUNG BILIARY STENT

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FGE·September 4, 2020

COTTON-LEUNG BILIARY STENT

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FGE·September 4, 2020

COTTON-LEUNG BILIARY STENT

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FGE·September 4, 2020

COTTON-LEUNG BILIARY STENT

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FGE·August 16, 2018

CYPHER SIROLIMUS-ELUTING CORONARY STENT

FDA Adverse Event
Injury ·CORDIS DE MEXICO·Product code NIQ·June 5, 2014

GORE HELEX SEPTAL OCCLUDER

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES·Product code MLV·November 27, 2012

TRILOGY O2

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code CBK·June 17, 2015