Denbur Inc

FDA Filings

This page includes the latest FDA filings for Denbur Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3006264569
FEI Number3006264569
NameDENBUR, INC.
Owner & OperatorDENBUR, INC.
Contact Address650 Blackhawk Drive --
Westmont IL 60559 US
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address650 Blackhawk Dr
WESTMONT, IL 60559 US
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
DENBUR, INC.
Multi-Brush Original Blue, Multi-Brush Multi-Colors, Magic-Brush, Nano-Brush, Maxi-Brush, Master-Brush, VO-Brush2007-04-09
DENBUR, INC.
Fracfinder2007-04-09
DENBUR, INC.
C-Flow, EZ-Flow, Den-Flow2007-04-09
DENBUR, INC.
Light-Tip2007-04-09

Related Finance Registrations
NCAGE Code0DZS8DENBUR INC
NCAGE Code5BCK2DENBUR INC.
CAGE Code0DZS8DENBUR INC
CAGE Code5BCK2DENBUR, INC.
DUNS166993717DENBUR, INC.
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