FDA.reportPublic FDA data

Kub Technologies, Inc.

Matched from indexed company URL: KUB Technologies, Inc.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30060511643006051164Kub Technologies, Inc.1N2026-01-01111 RESEARCH DR STRATFORD CT US 06615

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1002921341270945K210957Kubec Xpert 80 Radiography SystemMWP2021-08-31
1002921227672360K210956Kubtec Mozart (XPERT42)MWP2021-08-31
1002921265552961K210955Kubtec Mozart Supra (XPERT 84) Radiography SystemMWP2021-09-20
1002921447536999K200756Kubtec Mozart SupraMWP2020-06-12
1002921014349417K183624Kubtec Mozart (Xpert42)MWP2019-06-20
1002921798117477K151221Kubtec DIGIVIEW 395MQB2015-06-23
1002921394274029K141539KUBTEC X250IZL2014-10-29
1002921118579300K103348DIGIVIEW 250MQB2011-10-20
1002921022952137K083510KUBTEC XPERT 20KPR2009-01-08
1002922016668629K071233XPERT 40 SPECIMEN RADIOGRAPHY SYSTEMMWP2007-06-20
1002921422826022
1002921633635202

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
MWP62021-09-20
MQB22015-06-23
IZL12014-10-29
KPR12009-01-08

PMN#