COMPASS
LIVE

Serial Number

79429604

Owner

Compass HealthAI Applications Inc.

Filing Date

Feb 28, 2025

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COMPASS Trademark

Serial Number: 79429604

COMPASS is a trademark filed by Compass HealthAI Applications Inc. on February 28, 2025. The trademark is classified under Class 5 (Pharmaceuticals), Class 9 (Computers & Electronics), Class 10 (Medical Apparatus), Class 40 (Treatment & Processing), Class 41 (Education & Entertainment), Class 42 (Computer & Scientific), Class 44 (Medical Services). The application is currently pending registration.

Owner Contact Info

Compass HealthAI Applications Inc. (9 trademarks)

100-151 Charles St W

Entity Type: 03

Trademark Details

Filing Date

February 28, 2025

Registration Date

Not Registered

Goods & Services

Nutritional and nutraceutical supplements formulated to support ocular health, slow disease progression, and enhance retinal function, particularly for individuals diagnosed with late-stage macular disease or age-related macular degeneration (AMD).

Clinical and scientific research in the field of ophthalmology, focusing on the development, validation, and optimization of laser-based therapies, diagnostic devices, and minimally invasive interventions for retinal diseases; research and development (R&D) services aimed at advancing artificial intelligence (AI)-driven healthcare solutions, including predictive modeling, disease progression tracking, and outcome measurement in macular disease; providing online, non-downloadable software (SaaS/PaaS) with artificial intelligence (AI)-enabled analytics to support clinical decision-making, real-time patient monitoring, and health data management for improved vision care outcomes; technical consulting in the field of medical technology integration, including artificial intelligence (AI) algorithms, data analytics, and device interoperability for optimized patient care.

Downloadable software leveraging artificial intelligence (AI) algorithms for capturing, analyzing, and monitoring retinal images to assess disease progression, generate personalized treatment recommendations, and facilitate clinical decision-making; scientific and laboratory apparatus (not for direct clinical use) for collecting, interpreting, and managing research data related to ophthalmic treatments and disease models.

Minimally invasive laser-based apparatus for the treatment and management of late-stage macular disease, age-related macular degeneration (AMD), and low central vision, designed to improve or maintain visual acuity and patient quality of life; diagnostic instruments and devices, including handheld or wearable artificial intelligence (AI)-powered tools, for detecting, monitoring, and analyzing ocular conditions such as macular degeneration and other retinal disorders (term considered too vague by the International Bureau pursuant to Rule 13 (2) (b) of the Regulations); interventional medical devices tailored to stabilize or restore sight in individuals suffering from low vision due to advanced retinal pathology.

Custom manufacturing of ophthalmic devices, laser-based treatments, diagnostic equipment, and related components for third parties, ensuring adherence to quality, safety, and regulatory standards (term considered too vague by the International Bureau pursuant to Rule 13 (2) (b) of the Regulations).

Arranging and conducting seminars, webinars, workshops, and training programs for healthcare professionals and researchers on diagnosing, treating, and managing late-stage macular disease, age-related macular degeneration (AMD), and associated retinal conditions; publishing and distributing printed and electronic educational materials on best practices for ocular health maintenance, preventative eye care, and implementation of artificial intelligence (AI)-driven diagnostic and therapeutic approaches.

Providing minimally invasive ocular treatments, including laser-based therapies, to improve or stabilize visual acuity in patients with late-stage macular disease; telehealth and remote patient monitoring services that utilize artificial intelligence (AI)-driven platforms to guide clinical evaluations, detect disease changes, and optimize treatment regimens for individuals with low central vision; medical consultancy to physicians, clinics, and healthcare institutions on the adoption and integration of laser therapy, artificial intelligence (AI)-empowered diagnostic tools, and evidence-based nutraceutical protocols for retinal disease management.

Filing History

REFUSAL PROCESSED BY IB
Oct 18, 2025 RFNT
NON-FINAL ACTION MAILED - REFUSAL SENT TO IB
Sep 30, 2025 RFCS
REFUSAL PROCESSED BY MPU
Sep 30, 2025 RFRR
NON-FINAL ACTION (IB REFUSAL) PREPARED FOR REVIEW
Aug 19, 2025 RFCR
NON-FINAL ACTION WRITTEN
Aug 18, 2025 CNRT
ASSIGNED TO EXAMINER
Aug 15, 2025 DOCK
APPLICATION FILING RECEIPT MAILED
Aug 14, 2025 MAFR
NEW APPLICATION OFFICE SUPPLIED DATA ENTERED
Aug 14, 2025 NWOS
SN ASSIGNED FOR SECT 66A APPL FROM IB
Aug 7, 2025 REPR