10 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TRICON M TOTAL KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Ophthalmic Spatula
FDA UDI
KATENA PRODUCTS, INC.·00841668103371·CASTROVIEJO CYCLODIALYSIS SPATULA 0.25MM
UniTip Catheter
FDA UDI
Unisensor AG·07640172971673·
UniTip Catheter
FDA UDI
Unisensor AG·07640172973462·
STALIF C(R)
FDA 510(k)
FDA Class 2
·Orthopedic
ARIOL
FDA 510(k)
FDA Class 2
·Hematology
PROGRASP FORCEPS INSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·May 27, 2014
PINNACLE MTL INS NEUT36IDX520D
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code KWA·November 15, 2012
INSYNC III
FDA Adverse Event
Death
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWP·June 10, 2015
Vanguard XP Tibial Tray 71 mm Item # 195249
FDA Enforcement
Class II
·Terminated·Zimmer Biomet, Inc.·September 18, 2019