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Dado oficial do USPTO

ARC

Sabia que essa marca já está registrada no Estados Unidos?

Antes de investir em nome, identidade e divulgação, valide risco de colisão e estratégia de registro para não perder tempo nem budget.

Active USPTO registrationTipo: VerbalEscritório: US

Snapshot rápido

ARC

ST13

US500000079390974

Classe

9, 35, 41, 42, 44, 45

Pedido

79390974

Registro

8090389

Diagnóstico de risco e oportunidade

Leitura executiva para decisão de naming, protocolo e monitoramento.

Atenção: há risco ativo

Situação USPTO

Active USPTO registration

Tipo de processo

Pedido e registro

Eventos registrados

48

Atualização mais recente

30/07/2026

Classificação

Registrada

Tipo de marca

Verbal

Classes Nice

9, 35, 41, 42, 44, 45

Data de depósito

16/08/2023

Data de registro

06/01/2026

Data de expiração

-

Ação recomendada

Execute uma análise de colidência completa e valide classes antes de qualquer protocolo ou investimento de marca.

Próximo passo

Esses são os detalhes do processo de registro. Mesmo assim, o monitoramento constante é o que garante tranquilidade de que o seu principal ativo continue protegido.

Dados completos do processo

Campos estruturados da autoridade responsável e do histórico oficial.

Data da situação

06/01/2026

Última transação

30/07/2026

Escritório responsável

United States Patent and Trademark Office

Código da situação

700

Cadastro oficial

Principal Register

Código do desenho

4

Tipo de titular

99

Localização do titular

GB

Examinador

HACK, ANDREA R

Unidade examinadora

L80

Localização atual

GENERIC WEB UPDATE

Titulares e representantes

Titulares

ARC Regulatory Limited

Representantes

Amy L. Wright Taft Stettinius & Hollister LLP

Classificação técnica

Classes Nice

Classe 9Classe 35Classe 41Classe 42Classe 44Classe 45

Códigos Vienna

Sem códigos Vienna disponíveis.

Produtos e serviços

Classe 9

Computers, computer hardware and computer peripheral devices; computer software, computer application software, application software for mobile devices, all of the aforesaid being downloadable or recorded and for the purpose of accessing, navigating, analysing, updating and identifying regulatory and legislative requirements in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and law; Computer software, computer application software, application software for mobile devices, all of the aforesaid being downloadable or recorded and for the purpose of delivering training and educational content in respect of regulatory and legislative requirements in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and law; downloadable and recorded computer software for generating reports concerning regulatory requirements in the medical and life sciences industries; downloadable and recorded computer software for delivering training in relation to regulatory requirements in the medical and life sciences industries; downloadable publications, namely, magazines, newsletters, periodicals and brochures, all in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and law; downloadable and recorded media including written, image, video, audio and visual content, and infographics, namely e-books, CDs, DVDs, audio and video recordings, digital image files, podcasts and webinars in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and law; downloadable toolkits containing education, teaching and training resources comprised of downloadable guidelines, reports and data relating to regulatory compliance in the medical and life sciences industries; downloadable guidelines, reports and data relating to regulatory compliance in the medical and life sciences industries; none of the aforesaid relating to betting or gambling services; none of the aforesaid relating to AI technology specifically used in relation to player protection technology or risk reduction technology in the betting and gambling sector; none of the aforesaid in relation to the manufacture, provision, or supply of microprocessors, motherboard chipsets, network interface controllers and integrated circuits, flash memory, graphics chips, embedded processors nor other devices or software related to electronic design automation solutions and services

Classe 35

Business organization and administration, none of the foregoing in connection with the travel industry; providing office functions, none of the foregoing in connection with the travel industry; collection, compilation, analysis, reporting and dissemination of statistics, data and information, none of the foregoing in connection with the travel industry; business consulting and management in the field of clinical trials, namely, clinical data and regulatory submission management on behalf of medical, biopharmaceutical and biotechnology companies to assist them with clinical research, clinical trials and applications for drug approval; regulatory submission management, namely, assisting others in preparing and filing applications for regulatory approval of medical devices, medical technologies, medications, pharmaceuticals, and biotechnology; providing information online regarding preparing and filing applications for regulatory submission management; business and advisory consultancy services relating to obtaining and maintaining commercial product certifications

Classe 41

Education services, namely, providing training courses, online and live classes, seminars, webinars, workshops and tutorials in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and legal industries; providing of training in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and legal industries; education services in the medical and life sciences industries; educational services in relation to regulatory compliance, issues, updates and developments; educational services in relation to data integrity, unique device identification and regulatory readiness; education and training in relation to compliance and legal aspects of the European union In vitro Diagnostic Regulation; education services relating to quality services in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and legal industries; legal education services; publication of instructional literature, none of the foregoing in connection with the travel industry; publishing, reporting, and writing of texts, other than publicity texts, none of the foregoing in connection with the travel industry; arranging and conducting conferences, workshops, seminars, symposium, competitions, conventions and meetings in the medical and life sciences industries; writing, reporting and publication of non-downloadable guidelines, reports, data and case studies relating to the medical and life sciences industries; advisory and consultancy services relating to all abovementioned services; none of the aforesaid relating to betting or gambling services; none of the aforesaid relating to AI technology specifically used in relation to player protection technology or risk reduction technology in the betting and gambling sector.

Classe 42

Scientific, technological and industrial analysis, research and design services in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and legal industries; conducting and designing clinical trials for others; laboratory testing of materials; consultancy services related to laboratory testing of materials; clinical research in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and legal industries; biological research and medical research; site monitoring services; conducting early evaluations in the field of new pharmaceuticals; pharmaceutical product evaluation; product quality evaluation; quality control services for others; quality management services, namely, quality evaluation and analysis, quality assurance and quality control in the medical and life sciences industries; scientific research, analysis, testing, and related scientific studies in the medical and life sciences industries; consulting services in the medical and life sciences industries; biotechnology, biotechnology research consulting services; pharmaceutical research and product development for use in manufacturing; consulting services for others in the field of designing pre-clinical and clinical studies and trials for others; technical writing; technical writing for others; testing, analysis and evaluation of the services of others for the purpose of certification; testing of apparatus in the field of medical devices for certification purposes; electronic data storage; software as a service [SaaS] for the purpose of accessing, navigating, analysing, updating and identifying regulatory and legislative requirements in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and law; software as a service [SaaS] for the purpose of delivering training, educational content and reports in respect of regulatory and legislative requirements in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and law; providing online, non-downloadable software for the purpose of accessing, navigating, analysing, updating and identifying regulatory and legislative requirements in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and law; providing online, non-downloadable software for the purpose of delivering training, educational content and reports in respect of regulatory and legislative requirements in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and law; software design, development and engineering, none of the foregoing in connection with the travel industry; computer software consultancy, none of the foregoing in connection with the travel industry; providing online, nondownloadable software for generating reports concerning regulatory requirements in the medical and life sciences industries; providing online, non-downloadable software for delivering training in relation to regulatory requirements in the medical and life sciences industries; information, consultancy and advisory services relating to all abovementioned services; none of the aforesaid relating to betting or gambling services; none of the aforesaid relating to AI technology specifically used in relation to player protection technology or risk reduction technology in the betting and gambling sector; none of the foresaid in relation to the manufacture, provision, or supply of microprocessors, motherboard chipsets, network interface controllers and integrated circuits, flash memory, graphics chips, embedded processors nor other devices or software related to electronic design automation solutions and services.

Classe 44

Clinical medical consultation services; medical information; professional consultancy relating to health care; advisory services relating to medical and surgical instruments and devices; consulting and advisory services relating to obtaining and maintaining commerical product certifications for medical and surgical instruments and devices; consultancy and information services relating to medical, pharmaceutical and biopharmaceutical products; consulting and advisory services relating to the European Union in vitro diagnostic regulation (IVDR); consulting and advisory services relating to the European Union medical device regulation (MDR); consulting and advisory services relating to medical aspects of the European Union in vitro diagnostic regulation (IVDR); consulting and advisory services relating to medical aspects of the European Union medical device regulation (MDR); preparation of reports relating to medical matters; preparation of clinical and performance evaluation reports; preparation of clinical and performance evaluation reports for medical devices; information, consultancy and advisory services relating to all above mentioned services.

Classe 45

Legal services; regulatory and legal compliance auditing; advisory services relating to regulatory affairs; expert consultancy relating to legal issues regulatory compliance consulting services in the life sciences fields; regulatory compliance consulting services in the life sciences fields namely, reviewing standards and practices to assist others with compliance with governmental laws, regulations and rules pertaining to medical devices, medical technologies, medications, biopharmaceuticals, and biotechnology; consulting and advisory services relating to legal aspects of the European Union in vitro diagnostic regulation (IVDR); consulting and advisory services relating to legal aspects of the European Union medical device regulation (MDR); legal support services; information, consultancy and advisory services relating to all above mentioned services.

Publicações

Histórico de despachos e eventos da marca no USPTO.

48 publicações encontradas

FINO

FINAL DECISION TRANSACTION PROCESSED BY IB

30/07/2026

FICS

FINAL DISPOSITION NOTICE SENT TO IB

14/07/2026

FIMP

FINAL DISPOSITION PROCESSED

14/07/2026

NREP

NEW REPRESENTATIVE AT IB RECEIVED

07/05/2026

FICR

FINAL DISPOSITION NOTICE CREATED, TO BE SENT TO IB

06/04/2026

NRCC

NOTICE OF REGISTRATION CONFIRMATION EMAILED

06/01/2026

R.PR

REGISTERED-PRINCIPAL REGISTER

06/01/2026

CHPB

POST PUBLICATION AMENDMENT - ENTERED

17/12/2025

ETOP

EXTENSION OF TIME TO OPPOSE PROCESS - TERMINATED

14/12/2025

APET

ASSIGNED TO PETITION STAFF

11/12/2025

NREP

NEW REPRESENTATIVE AT IB RECEIVED

29/11/2025

DOCK

ASSIGNED TO EXAMINER

06/11/2025

EPPA

TEAS POST PUBLICATION AMENDMENT RECEIVED

24/10/2025

ETOF

EXTENSION OF TIME TO OPPOSE RECEIVED

26/08/2025

OPNX

NOTIFICATION OF POSSIBLE OPPOSITION - PROCESSED BY IB

22/08/2025

OPNS

NOTIFICATION OF POSSIBLE OPPOSITION SENT TO IB

06/08/2025

OPNR

NOTIFICATION OF POSSIBLE OPPOSITION CREATED, TO BE SENT TO IB

06/08/2025

NPUB

OFFICIAL GAZETTE PUBLICATION CONFIRMATION E-MAILED

05/08/2025

PUBO

PUBLISHED FOR OPPOSITION

05/08/2025

NONP

NOTIFICATION OF NOTICE OF PUBLICATION E-MAILED

30/07/2025

CNSA

APPROVED FOR PUB - PRINCIPAL REGISTER

01/07/2025

TEME

TEAS/EMAIL CORRESPONDENCE ENTERED

06/06/2025

CRFA

CORRESPONDENCE RECEIVED IN LAW OFFICE

06/06/2025

TROA

TEAS RESPONSE TO OFFICE ACTION RECEIVED

06/06/2025

CNRT

NON-FINAL ACTION WRITTEN

10/12/2024

LIME

LIMITATION FROM THE IB - REQUEST EXAM REVIEW

06/12/2024

LIMG

LIMITATION OF GOODS RECEIVED FROM IB

29/11/2024

XAEC

EXAMINER'S AMENDMENT ENTERED

15/11/2024

GNEN

NOTIFICATION OF EXAMINERS AMENDMENT E-MAILED

15/11/2024

GNEA

EXAMINERS AMENDMENT E-MAILED

15/11/2024

CNEA

EXAMINERS AMENDMENT -WRITTEN

15/11/2024

TEME

TEAS/EMAIL CORRESPONDENCE ENTERED

29/10/2024

CRFA

CORRESPONDENCE RECEIVED IN LAW OFFICE

29/10/2024

TROA

TEAS RESPONSE TO OFFICE ACTION RECEIVED

29/10/2024

RFNT

REFUSAL PROCESSED BY IB

23/06/2024

ADCH

CHANGE OF NAME/ADDRESS REC'D FROM IB

14/06/2024

RFCS

NON-FINAL ACTION MAILED - REFUSAL SENT TO IB

23/05/2024

RFRR

REFUSAL PROCESSED BY MPU

23/05/2024

RFCR

NON-FINAL ACTION (IB REFUSAL) PREPARED FOR REVIEW

11/05/2024

CNRT

NON-FINAL ACTION WRITTEN

10/05/2024

RFWR

NON-FINAL ACTION (IB REFUSAL) WITHDRAWN FOR REVIEW

10/05/2024

MAFR

APPLICATION FILING RECEIPT MAILED

24/04/2024

RFCR

NON-FINAL ACTION (IB REFUSAL) PREPARED FOR REVIEW

19/04/2024

CNRT

NON-FINAL ACTION WRITTEN

18/04/2024

DOCK

ASSIGNED TO EXAMINER

17/04/2024

NWOS

NEW APPLICATION OFFICE SUPPLIED DATA ENTERED

12/03/2024

NWOS

NEW APPLICATION OFFICE SUPPLIED DATA ENTERED

10/03/2024

REPR

SN ASSIGNED FOR SECT 66A APPL FROM IB

07/03/2024

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