6 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
ZEST IMPLANT ANCHOR
FDA 510(k)
FDA Class 2
·Dental
STRATO PLASTIC PORT INTRO KT(10 FR) LPS 7523/MODIF
FDA 510(k)
FDA Class 2
·General Hospital
TRIP CIC CATHETER
FDA 510(k)
FDA Class 1
·Gastroenterology, Urology
SPRINT QUATTRO SECURE
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·December 14, 2010
ASR UNI FEMORAL IMPL SIZE 47
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·January 22, 2013
QUARTET
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code OJX·July 10, 2014