6 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LEGIONELLA MWY SELECTIVE SUPPLEMENT
FDA 510(k)
FDA Class 1
·Microbiology
ORTHALIGN PLUS SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
SMITH AND NEPHEW TITANIUM INTERFERENCE SCREWS
FDA 510(k)
FDA Class 2
·Orthopedic
AXERA 2 ACCESS SYSTEM
FDA Adverse Event
Injury
·ARSTASIS, INC.·Product code DYB·March 30, 2014
SENSORMEDICS
FDA Adverse Event
Malfunction
·CAREFUSION·Product code LSZ·November 6, 2012
CABLE TENSIONER
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code LXH·June 12, 2015