GREENLIGHT GURU
Live / Registered — Registered (as of 17 Dec 2024)
What this means for you
Registered since 17 Dec 2024. The owner can stop confusingly similar uses in the classes it covers.
Record
- Serial number
- 97711061
- Registration number
- 7603481
- Mark type
- Stylized text
- Filed
- 09 Dec 2022
- Published for opposition
- 29 Oct 2024
- Registered
- 17 Dec 2024
- Attorney of record
- Kristin H. Hardy
Goods and services
- Class 035 — Advertising and business services: Business risk management services for medical device, life science, pharmaceutical, biotech, in vitro diagnostic device, and software as a medical device manufacturers in the fields of medical device manufacturing, life sciences medical device manufacturing, pharmaceutical manufacturing, biotech manufacturing, in vitro diagnostic device manufacturing, and software as a medical device manufacturing; business management and consulting services for medical device, life science, pharmaceutical, biotech, in vitro diagnostic device, and software as a medical device manufacturers for the fields of medical device manufacturing, life sciences medical device manufacturing, pharmaceutical manufacturing, biotech manufacturing, in vitro diagnostic device manufacturing, and software as a medical device manufacturing, namely, providing industry expertise and supplier management; records management services for medical device, life science, pharmaceutical, biotech, in vitro diagnostic device, and software as a medical device manufacturers, namely, document indexing for others in the fields of medical device manufacturing, life sciences medical device manufacturing, pharmaceutical manufacturing, biotech manufacturing, in vitro diagnostic device manufacturing, and software as a medical device manufacturing; regulatory information management services for medical device, life science, pharmaceutical, biotech, in vitro diagnostic device, and software as a medical device manufacturers in the fields of medical device manufacturing, life sciences medical device manufacturing, pharmaceutical manufacturing, biotech manufacturing, in vitro diagnostic device manufacturing, and software as a medical device manufacturing
- Class 045 — Legal and security services: Consulting services in the field of state and federal regulatory compliance requirements for medical device manufacturing, life sciences medical device manufacturing, pharmaceutical manufacturing, biotech manufacturing, in vitro diagnostic device manufacturing, and software as a medical device manufacturing; Tracking and monitoring regulatory requirements in the fields of medical device manufacturing, life sciences medical device manufacturing, pharmaceutical manufacturing, biotech manufacturing, in vitro diagnostic device manufacturing, and software as a medical device manufacturing for regulatory compliance purposes
Owner
- Soladoc, LLC, Indianpolis, IN, US
- Soladoc, LLC, Indianpolis, IN, US
- Soladoc, LLC, Indianpolis, IN, US
Prosecution history
- 17 Dec 2024 — NOTICE OF REGISTRATION CONFIRMATION EMAILED
- 17 Dec 2024 — REGISTERED-PRINCIPAL REGISTER
- 29 Oct 2024 — OFFICIAL GAZETTE PUBLICATION CONFIRMATION E-MAILED
- 29 Oct 2024 — PUBLISHED FOR OPPOSITION
- 09 Oct 2024 — NOTIFICATION OF NOTICE OF PUBLICATION E-MAILED
- 20 Sept 2024 — APPROVED FOR PUB - PRINCIPAL REGISTER
- 17 Aug 2024 — TEAS/EMAIL CORRESPONDENCE ENTERED
- 17 Aug 2024 — CORRESPONDENCE RECEIVED IN LAW OFFICE
- 17 Aug 2024 — ASSIGNED TO LIE
- 04 Mar 2024 — TEAS RESPONSE TO OFFICE ACTION RECEIVED
- 01 Dec 2023 — APPLICATION EXTENSION GRANTED/RECEIPT PROVIDED
- 01 Dec 2023 — APPLICATION EXTENSION TO RESPONSE PERIOD - RECEIVED
- 08 Sept 2023 — NOTIFICATION OF NON-FINAL ACTION E-MAILED
- 08 Sept 2023 — NON-FINAL ACTION E-MAILED
- 08 Sept 2023 — NON-FINAL ACTION WRITTEN