26 results
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25ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
BITEM ANGEL RELINE KIT, BITEM LABORATORY KIT, MODELS 120110, 120060
FDA 510(k)
FDA Class 2
·Dental
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450328033·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304131402·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304131563·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304131624·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304131464·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304131587·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304131600·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304131440·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304131426·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304131549·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304131488·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304131501·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304131525·
BLUE SKY BIO DENTAL IMPLANT SYSTEM
FDA 510(k)
FDA Class 2
·Dental
HL168B
FDA 510(k)
FDA Class 2
·Cardiovascular
TOTAL ASR FEM IMP SIZE 55
FDA Adverse Event
Injury
·DEPUY INTL., LTD. - 8010379·Product code KXA·September 10, 2013
DELTA SHUNT KIT, REGULAR, PL 1.5
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROSURGERY·Product code JXG·March 1, 2013
IN TOUCH ZU
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·March 3, 2011
WAVELIGHT FS200 FEMTOSECOND LASER
FDA Adverse Event
Injury
·WAVELIGHT GMBH·Product code LZS·July 21, 2014