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Kub Technologies, Inc.

USA · Stratford

✓ Record-verifiedregistrations found in 7 markets

This company has registrations in United States, Canada, Taiwan, Singapore, South Korea, Australia, Israel — 7 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable

CNChinaNMPA

n/aThis registry lists domestic registrants only

EUEuropean UnionEUDAMED

pendingnot queried

USUnited StatesFDA openFDA

6listed device types

Class I 2Class II 4Class III 0

plus 12 registration records and 10 510(k)

UKUnited KingdomMHRA PARD

pendingnot queried

BRBrazilANVISA

0registered devices

this export covers Class I / II only (the cadastro route)

SASaudi ArabiaSFDA

0registered imported devices

low-risk imported devices only; a 2023 snapshot, not updated since

CACanadaMDALL

1active device licences

Class II 1

11 including historic records

TWTaiwanTFDA

2valid device licences

Class II 2

SGSingaporeHSA SMDR

2device registrations

CLASS B 2

KRSouth KoreaMFDS GMP

1GMP quality-system certificates

Import 1

AUAustraliaTGA ARTG

2active ARTG entries

Class I 1IIa 1

HKHong KongMDACS

pendingnot queried

ILIsraelAMAR

3registrations

RURussiaRoszdravnadzor

pendingnot queried

Not yet connected: India CDSCO, Indonesia Kemenkes. The public search for Japan PMDA and Vietnam IMDA does not return manufacturer names, so entries cannot be linked to companies coming — where there is no data it is shown as "pending", never estimated.

How these numbers were verified

record-verified

Company-name search in every official database is a substring match and returns same-named but different companies. Each figure below is the count after re-checking every record against the manufacturer name.

United States12 registration records, 10 510(k), 0 PMA

Canada1 confirmed, 0 excluded

Manufacturer names merged into this page: Kub Technologies, Inc. · KUB TECHNOLOGIES, INC.

FDA 510(k) clearances by year

12007

12009

12011

12014

12015

12019

12020

32021

FDA listed device types

System, X-Ray, Stationary 1Cabinet, X-Ray System 1Solid State X-Ray Imager (Flat Panel/Digital Imager) 1System, X-Ray, Mobile 1Probe, Uptake, Nuclear 1Container, Specimen, Sterile 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K210955	Kubtec Mozart Supra (XPERT 84) Radiography System	2021-09-20
US	K210956	Kubtec Mozart (XPERT42)	2021-08-31
US	K210957	Kubec Xpert 80 Radiography System	2021-08-31
CA	89771	KUBTEC DIGIVIEW 250 - PORTABLE DIGITAL RADIOGRAPHY DETECTOR	Class II

Kub Technologies, Inc.

Registrations by market

How these numbers were verified

Company information

FDA 510(k) clearances by year

FDA listed device types

Registration details (sample)

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