6 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
.016' X .016 NICKEL TITANIUM UPRIGHTING SPRING
FDA 510(k)
FDA Class 1
·Dental
THE SUAD DEVICE
FDA 510(k)
FDA Class 2
·Dental
QUILL MONODERM KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BRAVO
FDA Adverse Event
Malfunction
·GIVEN IMAGING LTD.·Product code FFT·December 5, 2010
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·January 22, 2013
QUICK FLEX LV LEAD
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code OJX·July 9, 2014