7 results
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31ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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KARL STORZ SLOTTED WHISKER ARTHROSCOPIC BLADE
FDA 510(k)
FDA Class 2
·Orthopedic
EMPOWER CT/CTA INJECTOR SYSTEM, MODEL 9800/9900
FDA 510(k)
FDA Class 2
·Radiology
Hydris Oral Rinse
FDA 510(k)
FDA Unclassified
·Unknown
ACIST
FDA Adverse Event
Malfunction
·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·August 1, 2013
ITRAK 3500
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code LLZ·June 11, 2014
CORE SUMEX DRILL
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS KALAMAZOO·Product code ERL·January 24, 2013
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·January 18, 2011