6 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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AMMONIA TEST
FDA 510(k)
FDA Class 1
·Clinical Chemistry
LEUCADIA AUTOLOK PEDICLE SCREW SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
PROLITE PULSED LIGHT SYSTEM FOR THE REMOVAL OF UNWANTED HAIR
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
FLOGARD
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·May 15, 2014
CARELINK
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code KRG·October 31, 2012
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA·Product code NEK·June 2, 2015