7 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Interbody Fusion (IBF)/Vertebral Body Replacement (VBR) System
FDA 510(k)
FDA Class 2
·Orthopedic
MERIT MARQUIS FLOW SWITCH
FDA 510(k)
FDA Class 2
·Cardiovascular
PHOENIX HEMODIALYSIS DELIVERY SYSTEM, VERSION 3.35
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·July 2, 2025
RX ACCULINK CAROTID STENT SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code NIM·June 14, 2013
LIKO LIFT
FDA Adverse Event
Injury
·HILL-ROM CO·Product code FSA·July 18, 2011
CORFLO CUBBY LOW PROFILE GASTROSTOMY DEVICE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNT·September 16, 2008