8 results
·
22ms
·
Sources: EU EUDAMED, US FDA
STORZ DIAGNOSTIC MICROSCOPE SYSTEM
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
SURGISTAR
FDA UDI
SURGISTAR, INC.·00878799000958·
VISAGE PACS, VERSION 6.0/CS 3.1
FDA 510(k)
FDA Class 2
·Radiology
FIGURETRIM
FDA 510(k)
FDA Class 2
·Physical Medicine
POLYFLUX 210H
FDA Adverse Event
Injury
·GAMBRO DIALYSATOREN GMBH·Product code KDI·June 18, 2014
VIRTUOSO DR
FDA Adverse Event
Death
·MEDTRONIC MED REL, INC.·Product code LWS·October 26, 2010
VISIAN ICL (IMPLANTABLE COLLAMER LENS)
FDA Adverse Event
Malfunction
·STAAR SURGICAL COMPANY·Product code MTA·December 20, 2012
X-Celerator Hydrophilic Exchange Guidewire Catalog No. 103-0601-300 103-0601-350V10 103-0602-350V06 103-0601-300V01 103-0602-300 103-0602-350V09 103-0601-300V02 103-0602-300V01 103-0602-350V10 103-0601-300V03 103-0602-300V02 103-0601-300V06 103-0602-300v06 103-0601-300V10 103-0602-300V09 103-0601-300V11 103-0602-300V10 103-0601-350 103-0602-350 103-0601-350V01 103-0602-350V01 103-0601-350V06 103-0602-350V02
FDA Enforcement
Class I
·Terminated·Micro Therapeutics Inc, Dba Ev3 Neurovascular·November 16, 2016