7 results
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25ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NEXGEN COMPLETE KNEE SOLUTION
FDA 510(k)
FDA Class 2
·Orthopedic
BePOD® Foot Screws
FDA 510(k)
FDA Class 2
·Orthopedic
SOCK IT! ORAL PAIN GEL
FDA 510(k)
FDA Unclassified
·Unknown
MODIFIED KUGEL PATCH
FDA Adverse Event
Injury
·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·May 25, 2016
OPTIFLUX 180NRE DIALYZER FINISHED ASSY.
FDA Adverse Event
Malfunction
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code FJI·May 27, 2014
VERSACARE BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·January 29, 2013
INFUSOR LV5, 12 PK
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code MEB·January 18, 2011