Kub Technologies Inc

FDA Filings

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

FDA Registration(s)
Registration Number3006051164
FEI Number3006051164
NameKub Technologies, Inc.
Owner & OperatorKub Technologies
Contact Address111 Research Drive
Stratford CT 06615 US
Official Correspondent
  • Vikram Butani
  • x-203-3648544-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address111 RESEARCH DR
STRATFORD, CT 06615 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
KUB Technologies, Inc.
Kubtec Mozart Supra2020-06-12
KUB Technologies, Inc.
Kubtec Mozart (Xpert42)2019-06-20
Kub Technologies, Inc. [Kub Technologies]
KUBTEC GammaPRO2015-07-21
Kub Technologies, Inc. [Kub Technologies]
DIGIVIEW 3952015-07-17
KUB TECHNOLOGIES, INC
Kubtec DIGIVIEW 3952015-06-23
Kub Technologies, Inc. [Kub Technologies]
KUB 2502014-12-24
KUB TECHNOLOGIES, INC
KUBTEC X2502014-10-29
Kub Technologies, Inc. [Kub Technologies]
XPERT 802014-06-24
Kub Technologies, Inc. [Kub Technologies]
XPERT 80-L2014-06-24
Kub Technologies, Inc. [Kub Technologies]
MOZART2014-06-24
Kub Technologies, Inc. [Kub Technologies]
Digiview 2502011-11-09
KUB TECHNOLOGIES, INC
DIGIVIEW 2502011-10-20
Kub Technologies, Inc. [Kub Technologies]
Xpert 402009-02-20
Kub Technologies, Inc. [Kub Technologies]
Xpert 202009-02-20
KUB TECHNOLOGIES, INC
KUBTEC XPERT 202009-01-08
KUB TECHNOLOGIES, INC
XPERT 40 SPECIMEN RADIOGRAPHY SYSTEM2007-06-20

Related Finance Registrations

© 2020 FDA.report
This site is not affiliated with or endorsed by the FDA.