6 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ACTIFRESH 400 LENS
FDA 510(k)
FDA Class 2
·Ophthalmic
CALIX SPINAL IMPLANT SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Cruxcan (CRX-1000)
FDA 510(k)
FDA Class 2
·Dental
XIENCE PRIME EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code NIQ·February 28, 2013
INVACARE
FDA Adverse Event
Injury
·INVACARE·Product code ITI·February 7, 2011
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·UNKNOWN·Product code ITI·August 6, 2014