9 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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AltiVate Reverse® Glenoid
FDA 510(k)
FDA Class 2
·Orthopedic
SJM CONFIRM IMPLANTABLE CARDIAC MONITOR (ICM)
FDA 510(k)
FDA Class 2
·Cardiovascular
CryoVIVE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
GLIDEWELL HT IMPLANT Ø3.5 X 11.5 MM
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code DZE·August 5, 2025
GLIDEWELL HT IMPLANT Ø3.5 X 11.5 MM
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code DZE·August 5, 2025
GLIDEWELL HT IMPLANT Ø3.5 X 11.5 MM
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code DZE·October 21, 2024
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code OYC·November 6, 2014
ACCESS
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - AIBONITO·Product code FPA·September 2, 2011
ROTALINK? PLUS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - CORK·Product code MCX·July 18, 2013