6 results
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27ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
CONSENSUS ALL POLY TIBIA
FDA 510(k)
FDA Class 2
·Orthopedic
NuVasive Foundation-LL System
FDA 510(k)
FDA Class 2
·Orthopedic
DDRFORMULA AND DDRFORMULA PLUS
FDA 510(k)
FDA Class 2
·Radiology
ELECTRODE, PACEMAKER, PERMANENT
FDA Adverse Event
Injury
·MPRI·Product code DTB·February 9, 2013
SEVEN CONTINUOUS GLUCOSE MONITORING SENSOR
FDA Adverse Event
Other
·DEXCOM, INC.·Product code MDS·January 4, 2011
NONE
FDA Adverse Event
Malfunction
·Product code FNL·July 10, 2014