Legal Representation
Attorney
Sherry Metzger
USPTO Deadlines
Next Deadline
7 days remaining
Examiner's Amendment Completed
Due Date
July 23, 2025
Application History
23 events| Date | Code | Type | Description | Documents |
|---|---|---|---|---|
| Jul 8, 2025 | CNSA | O | APPROVED FOR PUB - PRINCIPAL REGISTER | Loading... |
| Jul 8, 2025 | GNEN | O | NOTIFICATION OF EXAMINERS AMENDMENT E-MAILED | Loading... |
| Jul 8, 2025 | CNEA | R | EXAMINERS AMENDMENT -WRITTEN | Loading... |
| Jul 8, 2025 | GNEA | F | EXAMINERS AMENDMENT E-MAILED | Loading... |
| Jul 8, 2025 | XAEC | I | EXAMINER'S AMENDMENT ENTERED | Loading... |
| Mar 19, 2025 | CFRC | R | SUBSEQUENT FINAL REFUSAL WRITTEN | Loading... |
| Mar 19, 2025 | GNSF | O | SUBSEQUENT FINAL EMAILED | Loading... |
| Mar 19, 2025 | GNS1 | O | NOTIFICATION OF SUBSEQUENT FINAL EMAILED | Loading... |
| Feb 10, 2025 | ERFR | I | TEAS REQUEST FOR RECONSIDERATION RECEIVED | Loading... |
| Feb 10, 2025 | TEME | I | TEAS/EMAIL CORRESPONDENCE ENTERED | Loading... |
| Feb 10, 2025 | CRFA | I | CORRESPONDENCE RECEIVED IN LAW OFFICE | Loading... |
| Jan 14, 2025 | GNFR | O | FINAL REFUSAL E-MAILED | Loading... |
| Jan 14, 2025 | GNFN | O | NOTIFICATION OF FINAL REFUSAL EMAILED | Loading... |
| Jan 14, 2025 | CNFR | R | FINAL REFUSAL WRITTEN | Loading... |
| Dec 5, 2024 | TROA | I | TEAS RESPONSE TO OFFICE ACTION RECEIVED | Loading... |
| Dec 5, 2024 | TEME | I | TEAS/EMAIL CORRESPONDENCE ENTERED | Loading... |
| Dec 5, 2024 | CRFA | I | CORRESPONDENCE RECEIVED IN LAW OFFICE | Loading... |
| Nov 14, 2024 | CNRT | R | NON-FINAL ACTION WRITTEN | Loading... |
| Nov 14, 2024 | GNRN | O | NOTIFICATION OF NON-FINAL ACTION E-MAILED | Loading... |
| Nov 14, 2024 | GNRT | F | NON-FINAL ACTION E-MAILED | Loading... |
| Nov 5, 2024 | DOCK | D | ASSIGNED TO EXAMINER | Loading... |
| Oct 10, 2024 | NWOS | I | NEW APPLICATION OFFICE SUPPLIED DATA ENTERED | Loading... |
| Apr 22, 2024 | NWAP | I | NEW APPLICATION ENTERED | Loading... |
Detailed Classifications
Class 042
Software as a service (SAAS) services featuring software for documenting and linking design control items during new product development; Software as a service (SAAS) services featuring software for manufacturing supplier management, product and regulatory certification management, product development task management, manufacturing specification management and delivery scheduling, all in the field of medical devices; Software as a service (SAAS) services featuring software for quality control auditing, risk scoring of device safety, supplier planning, incident management, complaint handling, adverse event and incident reporting, quality control inspections and assessments, quality system and cybersecurity program management, record keeping, regulatory intelligence, namely, tracking and complying with changes in regulations, all in the field of medical devices; Software as a service (SAAS) services featuring software for providing change management regulatory compliance document generation in the field of medical devices
First Use Anywhere:
Aug 20, 2023
First Use in Commerce:
Apr 20, 2024
Classification
International Classes
042