2,756 results
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25ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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SUNDT-KEES REINFORCING ANEURYSM CLIP
FDA 510(k)
FDA Class 2
·Neurology
SEMI-CONSTRAINT KEE JOINT HINGE PROSTH
FDA 510(k)
FDA Class 2
·Orthopedic
STENT PER 29MM 4-9MM MEDIUM
FDA Adverse Event
Injury
·CORDIS CORPORATION·Product code FGE·June 16, 2021
STENT PER 10MM MEDIUM
FDA Adverse Event
Death
·CARDINAL HEALTH MEXICO·Product code FGE·June 9, 2021
STENT PER 29MM 4-9MM MEDIUM
FDA Adverse Event
Injury
·CORDIS CORPORATION·Product code FGE·June 3, 2021
STENT PER 10MM MEDIUM
FDA Adverse Event
Injury
·CARDINAL HEALTH MEXICO·Product code FGE·June 8, 2021
STENT PER 15MM MEDIUM
FDA Adverse Event
Injury
·CARDINAL HEALTH MEXICO·Product code FGE·June 8, 2021
STENT PER 15MM MEDIUM
FDA Adverse Event
Injury
·CORDIS CORPORATION·Product code FGE·June 8, 2021
STENT PER 30MM 4.0MM LARGE
FDA Adverse Event
Injury
·CORDIS CORPORATION·Product code FGE·June 14, 2021
STENT PER 15MM MEDIUM
FDA Adverse Event
Injury
·CORDIS CORPORATION·Product code FGE·June 3, 2021
STENT PER 20MM 4-9MM MED
FDA Adverse Event
Injury
·CORDIS CORPORATION·Product code FGE·June 8, 2021
STENT PER 15MM MEDIUM
FDA Adverse Event
Injury
·CARDINAL HEALTH MEXICO·Product code FGE·June 9, 2021
EMPOWR PS KEE
FDA Adverse Event
Injury
·ENCORE MEDICAL L.P.·Product code JWH·March 16, 2020
ZIMMER(R) PERSONA THE PERSONALIZED KEE SYSTEM 14X +30MM TAPERED STEM EXTENSION
FDA 510(k)
FDA Class 2
·Orthopedic
UNKNOWN RIGHT KEE-BICOMP
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code JWH·March 27, 2017
ENDURANT STENT GRAFT
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·March 19, 2018
NCB, FEMUR PLATE, LEFT, 9 HOLES, 246 MM
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code HRS·December 13, 2018
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HRS·August 2, 2016
NAIL, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code JDS·August 2, 2016
NAIL, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code JDS·August 2, 2016