96 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ZAVATION CERVICAL PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
LEONE SPA
FDA UDI
LEONE SPA·08033707010036·CALIBRA 1ST MOLAR BANDS n.UL 30
Headed Screw Partially Threaded Short 3.0mm,30mm Length
FDA UDI
Pace Surgical, Inc.·00810211040227·Headed Screw Partially Threaded Short 3.0mm,30m...
PIPELINE
FDA UDI
Micro Therapeutics, Inc.·00847536008458·FA-71300-30 PIPELINE EMB DEVICE
Pipeline
FDA UDI
Micro Therapeutics, Inc.·00836462014756·Embolization Device
PIPELINE
FDA UDI
Micro Therapeutics, Inc.·00847536008434·FA-71300-30 PIPELINE EMB DEVICE
EXPECT ENDOSCOPIC ASPIRATION NEEDLE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
TAPERLOC COMPLETE SIZE 4MM AND XR 123
FDA 510(k)
FDA Class 2
·Orthopedic
NA
FDA UDI
STRYKER CORPORATION·04546540079572·8.0mm Acorn
NA
FDA UDI
STRYKER CORPORATION·04546540079541·6.5mm Acorn
NA
FDA UDI
STRYKER CORPORATION·04546540079558·7.0mm Acorn
NA
FDA UDI
STRYKER CORPORATION·04546540079534·6.0mm Acorn
NA
FDA UDI
STRYKER CORPORATION·04546540079565·7.5mm Acorn
NA
FDA UDI
STRYKER CORPORATION·04546540079589·9.0mm Acorn
NA
FDA UDI
STRYKER CORPORATION·04546540079527·5.0mm Acorn
NA
FDA UDI
STRYKER CORPORATION·04546540079510·4.0mm Acorn
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·REBEL PLATINUM CHROMIUM CORONARY STENT SYSTEM MONORAIL AND OVER THE WIRE
BUTTRESS/COMPRESSION NUT FOR 357.369
FDA Adverse Event
Malfunction
·SYNTHES BRANDYWINE·Product code HST·May 24, 2013
PARADIGM REAL -TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·September 19, 2014
TALENT THORACIC - XCELERANT
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR·Product code MIH·June 10, 2011