7 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LIBERTY ANTERIOR SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
LIBERTY POSTERIOR SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC INC.·Product code KWQ·February 11, 2010
SARNS RETROGRADE CANNULA
FDA 510(k)
FDA Class 2
·Cardiovascular
DIASTAT ANTI-LA (SS-B)
FDA 510(k)
FDA Class 2
·Immunology
REVEAL XT
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code DSI·February 15, 2013
ARTICULEZE M HEAD 36MM -2
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·July 29, 2014
PRECISION TEST STRIPS
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 20, 2011