29 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DENTALEYE 2 DENTAL IMAGE MANAGEMENT SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
Dornier MedTech
FDA UDI
Dornier MedTech GmbH·04049958002113·550 Micron 5X Reusable Lightguide, 150 watt, ba...
NC TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648151361·NC TREK Coronary Dilatation Catheter 3.50 mm x ...
NC TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648151408·NC TREK Coronary Dilatation Catheter 3.50 mm x ...
NC TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648151354·NC TREK Coronary Dilatation Catheter 3.50 mm x ...
NC TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648151392·NC TREK Coronary Dilatation Catheter 3.50 mm x ...
NC TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648151385·NC TREK Coronary Dilatation Catheter 3.50 mm x ...
NC TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648151378·NC TREK Coronary Dilatation Catheter 3.50 mm x ...
DISNEY
FDA UDI
FGX INTERNATIONAL INC.·00193033409121·
DISNEY
FDA UDI
FGX INTERNATIONAL INC.·00193033409138·
DISNEY
FDA UDI
FGX INTERNATIONAL INC.·00193033409114·
DISNEY
FDA UDI
FGX INTERNATIONAL INC.·00193033409091·
DISNEY
FDA UDI
FGX INTERNATIONAL INC.·00193033409107·
DISNEY
FDA UDI
FGX INTERNATIONAL INC.·00193033409084·
MODIFICATION TO BIOZ.COM HEMODYNAMIC MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
MAXITEX DUPLEX STERILE LATEX POWDERED SURGEON GLOVES WITH PROTEIN LABELING CLAIM (100 MICROGRAMS OR LESS)
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
UNKNOWN VERSASTEP
FDA Adverse Event
Malfunction
·COVIDIEN·Product code GCJ·June 11, 2015
DEPTH DEVICE, 2.7 / 3.5 / 4.0MM, LOW PRO
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HTJ·November 4, 2025
LOCKING SCREW, FULLY THREADED T2 TIBIA Ø5X45 MM
FDA Adverse Event
Malfunction
·STRYKER TRAUMA KIEL·Product code HSB·July 1, 2014
LOCKING SCREW, FULLY THREADED T2 TIBIA Ø5X45 MM
FDA Adverse Event
Malfunction
·STRYKER TRAUMA KIEL·Product code HSB·June 30, 2014