6 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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COMPASS(TM) STEREOTACTIC RETRACTOR SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
IMPACTOR FOR FEMORAL HEAD
FDA 510(k)
FDA Class 1
·Orthopedic
PATIENT EXAM GLOVES (MFG. NO. 1 FACTORY, WUHAN)
FDA 510(k)
FDA Class 1
·General Hospital
NATURALYTE
FDA Adverse Event
Death
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·June 13, 2014
QUICKFLEX XL LV LEAD
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·November 10, 2010
UNKNOWN REJUVENATE STEM
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS MAHWAH·Product code JDI·December 28, 2012