HEARGENE CONNECT
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HEARGENE CONNECT Trademark

Serial Number: 99834499

HEARGENE CONNECT is a trademark filed by U.S. Department of Health and Human Services on May 20, 2026. The trademark is classified under Class 9 (Computers & Electronics), Class 36 (Insurance & Financial), Class 41 (Education & Entertainment), Class 42 (Computer & Scientific), Class 44 (Medical Services), Class 16 (Paper Goods), Class 35 (Advertising & Business). The application is currently pending registration.

Owner Contact Info

U.S. Department of Health and Human Services (4 trademarks)

31 Center Drive
Bethesda, MD 208922111

Entity Type: 99

Trademark Details

Filing Date

May 20, 2026

Registration Date

Not Registered

Goods & Services

Providing grants and financial support for scientific and medical research and development in the fields of the phenotype, diagnosis, treatment, outcomes, study, and genetics of hearing loss, balance disorders, and associated medical conditions

Medical and scientific research in the fields of the phenotype, diagnosis, treatment, outcomes, study, and genetics of hearing loss, balance disorders, and associated medical conditions; medical and scientific research in the fields of design, planning, and implementation of longitudinal studies correlating genetic variants and hearing loss, balance disorders, and associated medical conditions; medical and scientific research, namely, planning and implementation of longitudinal studies correlating genetic variants and audiological data on hearing loss, balance disorders, and associated medical conditions; medical and scientific research in the fields of design, planning, and implementation of longitudinal studies for research and development of gene therapies for treating hearing loss, balance disorders, and associated medical conditions and identification of biomarkers associated therewith; medical and scientific research for long-term study of hearing loss, balance disorders, and associated medical conditions caused by genetic variants and/or physiological issues; medical and scientific research and development of the diagnosis and gene therapies for treating hearing loss, balance disorders, and associated medical conditions and for improving outcomes of treatments thereof; providing a website featuring medical and scientific research information in the fields of the phenotype, diagnosis, treatment, outcomes, study, and genetics of hearing loss, balance disorders, and associated medical conditions; providing medical and scientific research information; computer services, namely, creating an on-line community for registered users to participate in discussions and engage in social networking with others in connection with hearing loss, balance disorders, and other associated medical conditions, obtain information on specific forms of hearing loss, diagnosis, personalized information on treatments for and clinical trials aiming at treating hearing loss, balance disorders, and associated medical conditions; computer services, namely, creating an on-line community for researchers to identify etiology of hearing loss, balance disorders, and associated medical conditions; providing an internet website portal featuring information in the fields of the phenotype, diagnosis, treatment, outcomes, study, and genetics of hearing loss, balance disorders, and associated medical conditions; providing an internet website portal for screening and recruitment of individuals as research participants in longitudinal studies focusing on hearing loss, balance disorders, and associated medical conditions; providing an internet website portal for individuals with hearing loss and family members to consent to participate in medical research studies and record, track, upload and share reports of symptoms, familial information, and familial health; providing an internet website portal for individuals to share and receive information on the diagnosis, treatment, outcomes, study, and genetics of hearing loss, balance disorders, and associated medical conditions, and consent to genetic testing and share genetic testing results, obtain information about auditory and vestibular evaluations and inner ear imaging, obtain educational and counseling services about participants’ specific form of hearing loss and its etiology, receive personalized information on the availability of treatments and gene therapy studies and medical research opportunities that users may qualify for, receive study progress notifications, and participate in longitudinal studies focusing on hearing loss, balance disorders, and associated medical conditions; providing an internet website portal for providing information on personalized healthcare, counseling services, availability of treatments, research opportunities, and gene therapy studies in the fields of the phenotype, diagnosis, treatment, outcomes, study, and genetics of hearing loss, balance disorders, and associated medical conditions; genetic testing for scientific research and medical purposes

Electronic publications, namely, downloadable brochures, articles, factsheets, educational materials, video recordings, audio recordings, blogs, and podcasts in the fields of the phenotype, diagnosis, treatment, outcomes, study, and genetics of hearing loss, balance disorders, and associated medical conditions; downloadable videos in the fields of the phenotype, diagnosis, treatment, outcomes, study, and genetics of hearing loss, balance disorders, and associated medical conditions; downloadable computer application software for mobile phones, portable media players, handheld computers, wearable devices, laptops, and desktop computers, namely, software featuring information in the fields of the phenotype, diagnosis, treatment, outcomes, study, and genetics of hearing loss, balance disorders, and associated medical conditions; downloadable computer application software for mobile phones, portable media players, handheld computers, wearable devices, laptops, and desktop computers, namely, software for screening and recruitment of individuals as research participants in longitudinal studies focusing on hearing loss, balance disorders, and associated medical conditions; downloadable computer application software for mobile phones, portable media players, handheld computers, wearable devices, laptops, and desktop computers, namely, software for individuals with hearing loss and family members to consent to participate in medical research studies and record, track, upload and share reports of symptoms, familial information, and familial health; downloadable computer application software for mobile phones, portable media players, handheld computers, wearable devices, laptops, and desktop computers, namely, software for individuals to share and receive information on the diagnosis, treatment, outcomes, study, and genetics of hearing loss, balance disorders, and associated medical conditions, and consent to genetic testing and share genetic testing results, obtain information about auditory and vestibular evaluations and inner ear imaging, obtain educational and counseling services about participants’ specific form of hearing loss and its etiology, receive personalized information on the availability of treatments and gene therapy studies and medical research opportunities that users may qualify for, receive study progress notifications, and participate in longitudinal studies focusing on hearing loss, balance disorders, and associated medical conditions; downloadable computer application software for mobile phones, portable media players, handheld computers, wearable devices, laptops, and desktop computers, namely, software for providing information on personalized healthcare, counseling services, availability of treatments, research opportunities, and gene therapy studies in the fields of the phenotype, diagnosis, treatment, outcomes, study, and genetics of hearing loss, balance disorders, and associated medical conditions

Providing a registry and databases featuring information and data on hearing, audiology, inner ear imaging or radiology, balance, health, familial medical history, genetic diagnosis, and geographical location; providing a database featuring information and data on hearing, health, familial medical history, genetic diagnosis, biomarkers, and geographical location of individuals with hearing loss; providing a website featuring health information in the fields of the phenotype, diagnosis, treatment, outcomes, study, and genetics of hearing loss, balance disorders, and associated medical conditions; providing healthcare information; providing genetic diagnosis of hearing loss, balance disorders, and other associated medical conditions; health assessment services, namely, collecting, compiling, and analyzing genomic data and phenotypic data of individuals with hearing loss, balance disorders, and associated medical conditions; therapeutic evaluation and developments in the fields of the phenotype, diagnosis, treatment, outcomes, study, and genetics of hearing loss, balance disorders, and associated medical conditions

education services, namely, arranging and conducting training, workshops, seminars, webinars, and conferences in the fields of the phenotype, diagnosis, treatment, outcomes, study, and genetics of hearing loss, balance disorders, and associated medical conditions; education services, namely, providing educational, online, non-downloadable brochures, articles, factsheets, blogs, video recordings, audio recordings, podcasts, and social media posts in the fields of the phenotype, diagnosis, treatment, outcomes, study, and genetics of hearing loss, balance disorders, and associated medical conditions; Providing online publications, namely, questionnaires for collecting, compiling and analyzing health and genomic information and data on individuals with hearing loss, balance disorders, and associated medical conditions

Maintaining a registry of individuals with hearing loss, balance disorders, and associated medical conditions; maintaining databases containing deidentified information of individuals with hearing loss, balance disorders, and associated medical conditions; providing an on-line computer database featuring information in the fields of the phenotype, diagnosis, treatment, outcomes, study, and genetics of hearing loss, balance disorders, and associated medical conditions; maintaining a registry with personal information of participants for screening of individuals as research participants in studies and clinical trials focusing on hearing loss, balance disorders, and associated medical conditions; promoting public awareness of public-private partnerships in the fields of the phenotype, diagnosis, treatment, outcomes, study, and genetics of hearing loss, balance disorders, and associated medical conditions; promoting the interests of public-private partnerships in the fields of the phenotype, diagnosis, treatment, outcomes, study, and genetics of hearing loss, balance disorders, and associated medical conditions; promoting collaboration within the scientific, research, academic, health department, pharmaceutical, and clinical provider communities and industries to improve diagnosis, treatments, outcomes, and knowledge on the study and genetics of hearing loss, balance disorders, and associated medical conditions

Printed brochures, articles, and factsheets featuring information in the fields of the phenotype, diagnosis, treatment, outcomes, study, and genetics of hearing loss, balance disorders, and associated medical conditions

Filing History

APPLICATION FILING RECEIPT MAILED
May 20, 2026 MAFR
NEW APPLICATION ENTERED
May 20, 2026 NWAP