Trademark Search  /  GREENLIGHT GURU

GREENLIGHT GURU

● Live · Registered

U.S. federal trademark · Serial No. 97711061 · Reg. No. 7603481

Mark
GREENLIGHT GURU
Status
Registered
Serial Number
97711061
Registration No.
7603481
Filing Date
December 9, 2022
Registration Date
December 17, 2024
Class(es)
Class 035, Class 045

Owners

Soladoc, LLC
16 · Indianpolis, IN, US
Soladoc, LLC
16 · Indianpolis, IN, US
Soladoc, LLC
16 · Indianpolis, IN, US

Goods & 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

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

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Source: USPTO federal trademark records. Informational only, not legal advice. Status and details may lag the live USPTO database.