11 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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neo315
FDA 510(k)
FDA Class 2
·Radiology
Unity Total Knee System
FDA UDI
CORIN LTD·05056139232558·Patella Drill Guide Dome Sz 4 & 5
Mediflex 3.5mm Laparoscopic Instruments
FDA UDI
FLEXBAR MACHINE CORPORATION·00842102100437·Straight Dissector, w/ Flush Port & non-Lock Ha...
Intrigue
FDA UDI
LANCER ORTHODONTICS, INC.·00817573021192·INTRG WHISP ROTH BIC -7T 0A 022 UP
SURGRX ENSEAL VESSEL SEALING AND HEMOSTASIS SYSTEM INCLUDING THE ENSEAL CONTROLLER ADAPTER, ENSEAL OPEN AND LAPAROSCOPIS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
VIVORTE BVF LITE
FDA 510(k)
FDA Class 2
·Orthopedic
PROTEGE EVERFLEX SELF-EXPANDING STENT SYSTEM STANDARD
FDA Adverse Event
Death
·COVIDIEN·Product code FGE·April 17, 2018
PROTEGE EVERFLEX SELF-EXPANDING STENT SYSTEM STANDARD
FDA Adverse Event
Injury
·COVIDIEN·Product code FGE·April 17, 2018
NONE
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROSURGERY·Product code JXG·November 12, 2008
INTERSTIM
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·August 26, 2011
UNK
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·July 17, 2013