7 results
·
19ms
·
Sources: EU EUDAMED, US FDA
DIGITAL RING ELECTRDE
FDA 510(k)
FDA Class 2
·Neurology
SECURE Screw
FDA 510(k)
FDA Class 2
·Orthopedic
ORALUMINATOR III AUTO-LIGHT
FDA 510(k)
FDA Class 1
·Dental
HDI 5000 ULTRASOUND STANDARD SYSTEM
FDA Adverse Event
Malfunction
·PHILIPS ULTRASOUND, INC.·Product code IYO·March 30, 2012
NA
FDA Adverse Event
Malfunction
·STRYKER SUSTAINABILITY SOLUTIONS LAKELAND·Product code NUJ·March 6, 2013
CAPSUREFIX NOVUS
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011
SPRINT QUATTRO
FDA Adverse Event
Injury
·MPRI·Product code LWS·August 8, 2014