Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006051164

FEI Number

3006051164

Entity Name

Kub Technologies, Inc.

City/State/Country

STRATFORD, CT, US

Establishment Address

111 RESEARCH DR, STRATFORD, CT 06615, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Kub Technologies (Owner Number: 10028645)

Owner / Operator Contact Address

111 Research Drive, Stratford, CT 06615, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K210956

PMA Number

N/A

All Registered Proprietary Names

DIGIVIEW 395 XPERT84 MOZART SUPRA KUB 250 KUBBIE MOZART (XPERT42) Xpert 40 Xpert 20 Digiview 250 XPERT 80-L XPERT 80 MOZART KUBTEC GammaPRO XPERT80 XPERT42 MOZART

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MQB	Solid State X-Ray Imager (Flat Panel/Digital Imager)	Radiology	Class 2	892.1680	2015-07-17
MWP	Cabinet, X-Ray System	Radiology	Class 2	892.1680	2022-11-07
IZL	System, X-Ray, Mobile	Radiology	Class 2	892.1720	2014-12-24
FMH	Container, Specimen, Sterile	Pathology	Class 1	864.3250	2026-04-24
MWP	Cabinet, X-Ray System	Radiology	Class 2	892.1680	2020-07-17
KPR	System, X-Ray, Stationary	Radiology	Class 2	892.1680	2009-02-20
MQB	Solid State X-Ray Imager (Flat Panel/Digital Imager)	Radiology	Class 2	892.1680	2011-11-09
MWP	Cabinet, X-Ray System	Radiology	Class 2	892.1680	2014-06-24
IZD	Probe, Uptake, Nuclear	Radiology	Class 1	892.1320	2015-07-21
MWP	Cabinet, X-Ray System	Radiology	Class 2	892.1680	2022-11-07
MWP	Cabinet, X-Ray System	Radiology	Class 2	892.1680	2022-11-07

Official Correspondent

Vikram Butani

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Kub Technologies

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K070563	Vidar Systems Corp.	VIDAR VISION 2000	2007-03-16
K190691	Pixxgen Corporation	Pixx2430 Digital Diagnostic X-Ray Receptor Panel	2019-04-04
K150150	Rayence Co., Ltd.	1717SGN / 1717SCN Digital Flat Panel X-ray Detector	2015-03-27
K140771	Philips Medical Systems Dmc GmbH	PHILIPS ELEVA WORKSPOT	2014-04-25
K153059	Minxray, Inc.	HF1202H PowerPlus Portable X-ray Equipment	2016-02-02

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0005-2009	Toshiba American Medical Systems Inc	2	Toshiba Infinix fluoroscopy DFP-8000D Digital Radiography System with version 3.40 or higher software. Controller for Infinix interventional angiography systems.
Z-0031-2007	AGFA Corp.	2	CR DX-S, Image Intensified Fluoroscopic X-ray system.
Z-1470-2023	FUJIFILM Healthcare Americas Corporation	2	FujiFilm FDR AQRO (Model DR-XD1000)- A digital mobile X-ray system intended for use in general purpose radiography for generating radiographic images of human anatomy, including adult, pediatric, and neonatal exams
Z-3158-2024	FUJIFILM Healthcare Americas Corporation	2	The device is a mobile x-ray system designed to work with Fujifilm's GOS and CsI scintillator FDR D-EVO2 (DR-ID) 12XXSE) family of digital x-ray detectors coupled.
Z-0002-2009	GE Medical Systems, LLC	2	Revolution XR/d system control room PC model 5117866-2 with Software collector 5115434

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006051164. Last updated year: 2026. Please use registration number 3006051164 when referencing this establishment in official correspondence.