9 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
GE DATEX-OHMEDA AVANCE
FDA 510(k)
FDA Class 2
·Anesthesiology
CHLORAPREP ONE STEP CLEAR
FDA Adverse Event
Malfunction
·CAREFUSION 213, LLC 0113·Product code KXG·December 9, 2021
LINEAR? ST
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·October 8, 2025
MODIFICATION TO CENTAUR SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
MERITS HEALTH PRODUCTS OXYGEN CONCENTRATORS
FDA 510(k)
FDA Class 2
·Anesthesiology
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·February 2, 2026
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR LTD·Product code MCM·April 29, 2013
TRUETRACK
FDA Adverse Event
Malfunction
·NIPRO DIAGNOSTICS, INC.·Product code NBW·April 5, 2011
COSGROVE-EDWARDS ANNULOPLASTY SYSTEM
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code KRH·July 22, 2008