6 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SURGICAL INSTRUMENTS FOR USE W/ZIMMER
FDA 510(k)
FDA Class 2
·Orthopedic
THE AUTOTAC SYSTEM
FDA 510(k)
FDA Class 2
·Dental
VU C*POD INTERVERTEBRAL BODY FUSION DEVICE
FDA 510(k)
FDA Class 2
·Orthopedic
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 15, 2014
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC. USA·Product code LFR·October 22, 2007
INSYNC III
FDA Adverse Event
Injury
·MEDTRONIC S.A.·Product code DXY·October 31, 2012