Trademark Overview
On Wednesday, November 5, 2025, a trademark application was filed for LABRYTE with the United States Patent and Trademark Office. The USPTO has given the LABRYTE trademark a serial number of 99481748. The federal status of this trademark filing is NEW APPLICATION - RECORD INITIALIZED NOT ASSIGNED TO EXAMINER as of Wednesday, November 5, 2025. This trademark is owned by Helix Molecular Solutions LLC. The LABRYTE trademark is filed in the Computer & Software Products & Electrical & Scientific Products, Advertising, Business and Retail Services, Education & Entertainment Services, Computer & Software Services & Scientific Services, Personal, and Legal & Social Services categories with the following description:
Educational services, namely, conducting workshops, webinars, training programs, and continuing education courses in the field of molecular diagnostics, laboratory compliance, biotechnology, regenerative medicine, and pharmaceutical development and distribution of educational materials in connection therewith; Education services, namely, providing workshops, webinars, training programs, and continuing education courses in the field of molecular diagnostics, laboratory compliance, biotechnology, regenerative medicine, and pharmaceutical development; Providing online non-downloadable electronic publications in the nature of training manuals, validation guides, and compliance workbooks in the field of laboratory and biotechnology consulting; Providing educational mentoring services and programs in the field of science, technology, engineering, and mathematics (STEM), with a focus on laboratory sciences, method validations, and regulatory compliance; Training services in the field of scien...
Scientific research consulting in the field of molecular diagnostics, biotechnology, regenerative medicine, and life sciences companies; Technological consultation in the technology field of molecular diagnostics, biotechnology, regenerative medicine, and pharmaceuticals; Consulting services for others in the field of design, planning, and implementation project management of setup, validation, and compliance of CLIA-certified laboratories, GMP facilities, and FDA-regulated manufacturing sites; Scientific research consulting in the field of assay, biologic, and drug product development, including molecular diagnostics, stem cells, exosomes, amniotic allografts, and exosome-based drug delivery platforms; Scientific research consulting in the field of method validations, laboratory information systems, document control, quality management systems, and regulatory documentation; Technological consultation in the technology field of biotechnology, pharmaceutical, and regernative medicine co...
Downloadable computer software for use in laboratory information management, quality assurance, document control, electronic quality management (eQMS), and regulatory compliance in the fields of clinical diagnostics, biotechnology, regenerative medicine, and pharmaceutical development; Downloadable computer software for managing laboratory workflows, coordinating clinical studies, integrating regulatory documentation, and supporting GMP compliance
Business consulting services in the field of clinical diagnostics, biotechnology, regenerative medicine, and pharmaceutical development; Business management consulting and advisory services for the diagnostic laboratories, GMP facilities, and companies developing assays, instruments, stem cell products, exosome-based products, tissue-derived biologics, and drug delivery platforms industry; Business project management services; Business management consulting and advisory services for the laboratory and manufacturing facility build-outs, including planning, contractor coordination, and vendor engagement industry; Business consulting services; Business consulting services in the field of staffing, recruiting, marketing, commercialization strategy, mock audits, laboratory workflow reviews, and B2B networking for laboratory, biotechnology, pharmaceutical, and life sciences companies
Regulatory compliance consulting in the field of clinical laboratories, biotechnology companies, regenerative medicine organizations, and pharmaceutical developers in connection with CLIA, CAP, GMP, and FDA standards; Regulatory compliance consulting in the field of project management relating to diagnostic assays, medical devices, biologics, stem cells, exosomes, tissue-derived products, drug delivery platforms, and mock audits or pre-inspection readiness reviews; Regulatory compliance consulting in the field of laboratory, biotechnology, and pharmaceutical companies, namely, reviewing standards and practices to assure compliance with governmental regulations and industry standards
