6 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ATLAS III ACETABULAR CUP
FDA 510(k)
FDA Class 2
·Orthopedic
SEARS MODEL LM9091 IN-THE-EAR HEARING INSTRUMENT
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
SARNS PORTABLE POWER MODULE
FDA 510(k)
FDA Class 2
·Cardiovascular
TRANSTAR STRETCHER
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FPO·January 17, 2013
ICL (IMPLANTABLE COLLAMER LENS)
FDA Adverse Event
Injury
·STAAR SURGICAL CO.·Product code MTA·January 7, 2011
ASP AUTOMATIC ENDOSCOPE REPROCESSOR WITH PRINTER
FDA Adverse Event
Malfunction
·MINNTECH CORPORATION·Product code KOG·July 28, 2014