42 results
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33ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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EnSite X EP System, Advisor VL Circular Mapping Catheter, Sensor Enabled, Advisor FL Circular Mapping Catheter, Sensor Enabled, Advisor HD Grid High Density Mapping Catheter, Senor Enabled
FDA 510(k)
FDA Class 2
·Cardiovascular
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112496·BARRON VACUUM TREPHINE 7.5MM
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112533·BARRON VACUUM TREPHINE 8.5MM
SprintRay High Impact Denture Teeth - A1
FDA UDI
Sprintray, Inc.·00850039704307·SprintRay High Impact Denture Teeth is a light-...
FREEZER TEETHER
FDA 510(k)
FDA Class 2
·Dental
REGISTRADO X-TRA
FDA 510(k)
FDA Class 2
·Dental
Trabecular Metal®
FDA UDI
Zimmer, Inc.·00889024119079·
Trabecular Metal®
FDA UDI
Zimmer, Inc.·00889024119086·
Trabecular Metal®
FDA UDI
Zimmer, Inc.·00889024119093·
UNKNOWN LIGASURE INSTRUMENT
FDA Adverse Event
Injury
·COVIDIEN MFG DC BOULDER·Product code GEI·October 21, 2020
ENDURANT STENT GRAFT
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code MIH·September 29, 2020
TALENT AAA STENT GRAFT
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·September 29, 2020
TALENT AAA STENT GRAFT
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code MIH·September 29, 2020
ENDURANT STENT GRAFT
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·September 29, 2020
ENDURANT STENT GRAFT
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code MIH·September 29, 2020
ENDURANT STENT GRAFT
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·September 29, 2020
OXIMAX N-595 PULSE OXIMETER
FDA Adverse Event
Malfunction
·COVIDIEN FORMERLY TYCO HEALTHCARE·Product code DQA·October 15, 2008
HEARTMATE II LVAS
FDA Adverse Event
Injury
·THORATEC CORP.·Product code DSQ·June 27, 2013
ANEURX AAADVANTAGE STENT GRAFT SYSTEM - HYDRO
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR·Product code MIH·August 5, 2011
Barron Radial Vacuum Trephine (1) Complete Trephine Set 9.0mm Dia. Ref. K20-2062 Lot 122336 Opthalmic
FDA Recall
Terminated
·Surgical Instrument Service And Savings, Inc.·Product code HRH·May 3, 2013