36 results
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33ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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e-Ortho Shoulder Software
FDA 510(k)
FDA Class 2
·Radiology
DJO SURGICAL
FDA UDI
Encore Medical, L.P.·00190446924470·SPECIAL, DAA NEBULA OFFSET STEM INSERTER
NA
FDA UDI
Synthes GmbH·20887587028634·2.0MM IMF SCREW SELF-DRILLING 8MM
Blade Handle
FDA UDI
KATENA PRODUCTS, INC.·00841668112373·CHUCK HANDLE #3KA 7.5CM LONG
SIGMA
FDA 510(k)
FDA Class 2
·Dental
SYNTHES (USA) RESORBABLE FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Dental
MEDTRONIC
FDA Adverse Event
Malfunction
·MEDTRONIC·Product code FPA·July 17, 2009
AXIOM PX IMPLANT
FDA Adverse Event
Injury
·ANTHOGYR·Product code DZE·September 2, 2019
XEN 45 GTS
FDA Adverse Event
Injury
·ALLERGAN (IRVINE)·Product code KYF·May 30, 2019
WATCHMAN LAA CLOSURE DEVICE & DELIVERY SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code NGV·February 6, 2019
AXIOM REG IMPLANT
FDA Adverse Event
Injury
·ANTHOGYR·Product code DZE·September 11, 2019
AXIOM REG IMPLANT
FDA Adverse Event
Injury
·ANTHOGYR·Product code DZE·July 31, 2019
ATTAIN ABILITY
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code OJX·August 11, 2011
MOTORIZED 3-WHEELED VEHICLE FOR OUTSIDE TRANSPORT
FDA Adverse Event
C.T.M. SHANGHAI·Product code INI·October 27, 2014
GRAFTMASTER RX CORONARY STENT GRAFT SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MAF·July 2, 2013
WATCHMAN LAA CLOSURE DEVICE & DELIVERY SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code NGV·February 6, 2019
EVOLUT R TRANSCATHETER AORTIC VALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·January 8, 2020
COREVALVE TRANSCATHETER AORTIC VALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·January 8, 2020
INDUCTIGRAFT
FDA Adverse Event
Injury
·BAXTER HEALTHCARE CORPORATION·Product code MQV·April 14, 2020
MICRA
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code PNJ·April 30, 2020