8 results
·
22ms
·
Sources: EU EUDAMED, US FDA
ML-800 AUTOELECTRONIC LIGHT SOURCE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
KYPH X HV-R BONE CEMENT
FDA 510(k)
FDA Class 2
·Orthopedic
THERACARD 400
FDA 510(k)
FDA Class 2
·Cardiovascular
KYPHX® HV-R? BONE CEMENT
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code NDN·March 14, 2014
KYPHX® HV-R? BONE CEMENT
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code NDN·June 20, 2014
ESSURE
FDA Adverse Event
Injury
·BAYER·Product code HHS·June 18, 2014
CARPENTIER-EDWARDS PERIMOUNT MAGNA PERICARDIAL BIOPROSTHESIS
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·January 2, 2013
BIVONA TTS TRACHEOSTOMY TUBE
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC·Product code JOH·November 1, 2010