7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ORTHO* SERUM ELISA TEST SYSTEM
FDA 510(k)
FDA Class 2
·Immunology
EXTREMITY MEDICAL HAMMERTOE DEVICE
FDA 510(k)
FDA Class 2
·Orthopedic
AMS LARGE PORE POLYPROPYLENE MESH
FDA 510(k)
FDA Class 3
·Obstetrics/Gynecology
START-X TIP EMS INSERT 3
FDA Adverse Event
Malfunction
·MAILLEFER INSTRUMENTS HOLDING SARL·Product code ELC·November 20, 2024
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·May 27, 2014
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·November 15, 2012
VISIAN ICL (IMPLANTABLE COLLAMER LENS)
FDA Adverse Event
Injury
·STAAR SURGICAL CO.·Product code MTA·September 8, 2010