7 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HOWMEDICA AND HOWMEDICA LEIBINGER BONE SCREW WASHERS
FDA 510(k)
FDA Class 2
·Orthopedic
FINDRWIRZ GUIDE WIRE SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
HD LifeSciences Cervical IBFD System
FDA 510(k)
FDA Class 2
·Orthopedic
ARCHITECT C4000 SYSTEM
FDA Adverse Event
Malfunction
·ABBOTT MANUFACTURING INC·Product code JJE·July 31, 2018
NATURALYTE
FDA Adverse Event
Death
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·June 25, 2014
2520274-2013-10524
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code MNI·February 22, 2013
SOLETRA
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code MHY·February 3, 2011