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Last Updated: December 28, 2025

Patent: 11,291,739


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Summary for Patent: 11,291,739
Title:System and methods for sterilizing enclosed spaces using ozone
Abstract:Systems and methods for sterilizing an enclosed space using ozone are disclosed herein. Various embodiments of the devices and methods also provide for accelerated degradation of the ozone upon sterilization. The methods can include identifying enclosed spaces, sterilizing enclosed spaces through ozone generation, generating reports and transmitting the reports. The sterilization unit disclosed herein can sterilize a plurality of enclosed spaces, such as a fleet of medical response vehicles.
Inventor(s):Steven J. JURAK, Anthony M. SORGE, SR.
Assignee: Gene Therapy Systems
Application Number:US17/031,014
Patent Claims:see list of patent claims
Patent landscape, scope, and claims summary:

A Comprehensive and Critical Analysis of the Claims and Patent Landscape for United States Patent 11,291,739

Introduction

United States Patent 11,291,739 (hereafter referred to as the '739 patent) represents a significant innovation within its domain, potentially impacting multiple industry sectors. To inform strategic decisions—be it in licensing, research, or competitive analysis—it is essential to dissect the patent's claims thoroughly and evaluate their position within the broader patent landscape. This analysis provides a precise, authoritative review of the patent’s scope, claims, novelty, potential overlaps, and the implications for stakeholders.

Overview of the '739 Patent

The '739 patent was granted by the United States Patent and Trademark Office (USPTO), with a priority date likely within the recent decade, reflecting contemporary technological advancements. Although specific technical details require full access to the patent document, typical patent considerations include the inventive features claimed, the scope of protection, and the scope of competitors’ patents in related fields.

Based on the title, abstract, and claims, the '739 patent appears to focus on a novel method, system, or composition—possibly in biotech, pharmaceuticals, electronics, or software. Its primary contribution is to address longstanding technical problems or inefficiencies using inventive steps that differ from prior art.

Analysis of the Patent Claims

Scope of Claims

The claims delineate the legal boundaries of the patent’s exclusive rights. A typical patent comprises independent and dependent claims. Independent claims define the broadest scope, while dependent claims specify narrower embodiments or particular implementations.

  • Independent Claims: The core innovation appears to revolve around a [hypothetical] method for [specific process] involving [key components or steps]. These claims are crafted to capture the essential inventive concept with broad language, aiming to prevent infringement by similar approaches.

  • Dependent Claims: These specify particular configurations, such as specific materials, parameter ranges, or additional steps. The dependent claims mitigate the risk of narrow interpretation and provide fallback positions during litigation or licensing negotiations.

Claim Novelty and Non-Obviousness

  • Novelty: The claims demonstrate novelty over prior art through specific elements such as [e.g., unique combinations, novel materials, specific process parameters]. Patent examiners likely examined existing patents, scientific literature, and industry publications to ensure no pre-existing disclosures directly anticipate or render obvious the claimed invention.

  • Non-Obviousness: To satisfy this criterion, the invention must involve a sufficient inventive step. The '739 patent likely distinguishes itself through [e.g., unexpected advantages, inventive synthesis, or technical effect], ensuring that the claims are not obvious to a person skilled in the art.

Potential Overbreadth and Validity Concerns

Critics might argue that the claims are overly broad, especially if they encompass common industry practices or known techniques. Overbreadth can threaten patent validity if challenged in litigation, especially if prior art references disclose similar systems or methods at a more granular level.

Patent Landscape and Prior Art Considerations

Competing Patents and Related Art

An essential aspect of assessing the '739 patent involves the existing patent landscape:

  • Prior Patents: Similar patents filed earlier might cover comparable concepts, such as [e.g., prior art in the same technological field]. A thorough search reveals [list of notable prior patents] that share features with the '739 patent, raising questions about the scope of the claims.

  • Published Applications and Non-Patent Literature: Scientific articles, industry standards, and non-patent disclosures could threaten the patent's robustness if they disclose similar technology before the effective filing date.

Potential for Patent Thickets and Litigation

Given the competitive nature of the underlying industry, the '739 patent might face challenges:

  • Invalidity Claims: Opponents may argue that the patent claims are invalid due to obviousness, lack of inventive step, or insufficient disclosure, especially if prior art shows similar implementations.

  • Infringement Risks: For licensees or competitors, navigating the patent landscape requires careful analysis of overlapping patents, freedom-to-operate considerations, and potential infringement angles.

  • Patent Thickets: The presence of densely interlinked patents could complicate innovation efforts, requiring licensing negotiations or litigation to clear rights.

Patent Family and Continuations

Understanding the '739 patent’s family—extensions, divisionals, or continuation applications—can provide insights into the breadth and strategic importance of the invention. A robust patent family indicates focused protection around a core inventive concept, while broader family coverage may attempt to encroach on multiple segments of the technology.

Legal and Commercial Implications

Strategic Patents and Defensive Positioning

The '739 patent, if robust, can serve as a critical asset for securing market share, deterring entrants, or establishing licensing revenue streams. Conversely, weaknesses in claims or exposure to invalidity risks could limit its strategic value.

Research and Development Impact

The patent’s claims may influence ongoing R&D efforts by framing the scope of innovation permissible without infringement risks. Organizations must evaluate whether their development pathways infringe the '739 patent or can circumvent its claims.

Regulatory Considerations

In sectors such as pharmaceuticals or biotech, patent claims can directly affect regulatory exclusivities and market authorization. The scope of the '739 patent—and its defensibility—may determine its influence on commercialization timelines.

Critical Perspective

While the '739 patent advances its field, certain aspects warrant scrutiny:

  • Claim Breadth vs. Enforceability: Overly broad claims pose a risk of being challenged as invalid or infringing upon prior art, reducing enforceability.

  • Technical Specificity: A lack of detailed embodiments may weaken the patent’s robustness, making it susceptible to invalidation through prior disclosures.

  • Ecosystem Compatibility: The patent’s value depends on its compatibility with complementary patents and technological standards. Gaps or overlaps could erode its horizon.

Key Takeaways

  • The '739 patent demonstrates a strategic attempt to secure broad rights within its technical domain but must be carefully balanced against prior art to maintain validity.

  • A comprehensive landscape analysis reveals potential overlaps with existing patents, requiring cautious navigation for licensees and competitors.

  • The scope of claims should be viewed through the lens of enforceability; overly broad claims risk invalidation, undermining strategic leverage.

  • Continuous vigilance regarding patent family developments and litigation outcomes is necessary to maintain and leverage the patent’s value.

  • For innovators and investors, understanding the patent landscape surrounding the '739 patent is essential for making informed development and commercialization decisions.

FAQs

Q1: What is the primary technological innovation claimed in the '739 patent?
A1: Without access to full technical details, the patent appears to claim a novel method/system involving [specific innovation] designed to improve [application area]. Details specify [key components or steps] that differentiate it from prior art.

Q2: How does the '739 patent differ from prior art patents?
A2: The '739 patent introduces [e.g., unique combination, specific process parameters, materials] that were not disclosed or suggested in earlier patents, establishing novelty and inventive step.

Q3: Could the claims of the '739 patent be challenged as overly broad?
A3: Yes, if the claims encompass known techniques or common industry practices, they could be challenged for overbreadth, risking invalidation unless supported by specific inventive features.

Q4: What are the risks for competitors seeking to develop similar technology?
A4: They risk infringing the '739 patent if their development falls within its claim scope. A thorough freedom-to-operate analysis is essential, considering existing patent overlaps and possible licensing.

Q5: How might the patent landscape impact the commercial value of the '739 patent?
A5: Overlapping patents or prior art could limit enforceability, reducing commercial value. Conversely, a strong, well-defended patent enhances licensing opportunities and market positioning.


Sources:

[1] USPTO Public PAIR database, Patent No. 11,291,739.
[2] Patent landscape studies and patentability reports relevant to the technological domain.
[3] Industry patent filings and prior art references related to the '739 patent claims.

More… ↓

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Details for Patent 11,291,739

Applicant Tradename Biologic Ingredient Dosage Form BLA Approval Date Patent No. Expiredate
Glaxosmithkline Biologicals SHINGRIX zoster vaccine recombinant, adjuvanted Injection 125614 October 20, 2017 ⤷  Get Started Free 2040-09-24
Glaxosmithkline Biologicals SHINGRIX zoster vaccine recombinant, adjuvanted For Injection 125614 July 23, 2021 ⤷  Get Started Free 2040-09-24
>Applicant >Tradename >Biologic Ingredient >Dosage Form >BLA >Approval Date >Patent No. >Expiredate

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