9 results
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36ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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E-CUBE 11
FDA 510(k)
FDA Class 2
·Radiology
AEQUALIS REVERSED PROSTHESIS
FDA 510(k)
FDA Class 2
·Orthopedic
CODONICS SAFE LABELING SYSTEM (SLS), MODEL 500I/500P
FDA 510(k)
FDA Class 2
·Anesthesiology
PS TIBIAL INSERTS SZ 3, 13MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·May 1, 2023
ZILVER FLEX 35 VASCULAR SELF-EXPANDING STENT
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code NIO·April 22, 2020
CAPSUREFIX NOVUS
FDA Adverse Event
Injury
·MPRI·Product code DTB·October 10, 2014
GYNECARE GYNEMESH* PS
FDA Adverse Event
Injury
·ETHICON, INC.·Product code OTO·June 11, 2013
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 14, 2011
VALIANT STENT GRAFT
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·August 1, 2017