8 results
·
20ms
·
Sources: EU EUDAMED, US FDA
ENDO-CORE
FDA 510(k)
FDA Class 1
·Dental
"2.7MM" SYSTEM
FDA UDI
BIOMET MICROFIXATION, INC·00888233011945·
"2.7MM" SYSTEM
FDA UDI
BIOMET MICROFIXATION, INC·00841036152796·
MCKESSON HORIZON CARDIOLOGY
FDA 510(k)
FDA Class 2
·Radiology
TULSA CONTRA ANGLES
FDA 510(k)
FDA Class 1
·Dental
ON-Q PAIN PUMP
FDA Adverse Event
Injury
·I-FLOW, LLC·Product code MEB·January 8, 2013
UNKNOWN
FDA Adverse Event
Other
·ENCORE MEDICAL, L.P.·Product code JDI·November 2, 2010
PULSE GEN MODEL 103
FDA Adverse Event
Malfunction
·CYBERONICS INC·Product code LYJ·July 3, 2014