18 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CapLOX II®/TowerLOX® MIS Pedicle Screw System
FDA 510(k)
FDA Class 2
·Orthopedic
CHIMAERA Hip Fracture System
FDA UDI
ORTHOFIX SRL·18054242515456·ENTRY REAMER
POWDER-FREE VINYL PATIENT EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
INSTINCT JAVA SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·July 23, 2025
HIGH DEFINITION LCD MONITOR
FDA Adverse Event
Malfunction
·SHIRAKAWA OLYMPUS CO., LTD.·Product code FET·November 10, 2025
FLEXIMA BILIARY STENT SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code FGE·October 7, 2008
IAB: 7.5 FR - 30CC
FDA Adverse Event
Malfunction
·ARROW INTL., INC.·Product code DSP·July 13, 2011
EXTENS. Ø1.5 L400 F/GUIDEWIRE NO. 03.630
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code LRN·June 27, 2013
INSTINCT JAVA SCREW, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER SPINE·Product code MNH·October 30, 2019
INSTINCT JAVA SCREW, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER SPINE·Product code MNH·October 30, 2019
INSTINCT JAVA SCREW, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER SPINE·Product code MNH·October 30, 2019
INSTINCT JAVA ROD, UNKNOWN
FDA Adverse Event
Injury
·ZIMMER SPINE·Product code MNH·October 30, 2019
INSTINCT JAVA ROD, UNKNOWN
FDA Adverse Event
Injury
·ZIMMER SPINE·Product code MNH·October 31, 2019
M2A MAGNUM PF CUP 56MM O.D. X 50 I.D.
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·September 28, 2016
INSTINCT JAVA SCREW, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER SPINE·Product code MNH·October 31, 2019
M2A MAGNUM TAPER ADAPATER 42-50MM PLUS 3MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·September 28, 2016
MODULAR TAPERLOC FEMORAL POROUS COATED 10.0 X 140MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LPH·September 28, 2016