Six companies met our criteria from the nine 10-K annual reports filed with the SEC on 18 June 2026. To qualify, a company must have filed an annual 10-K report on the target date and have a prior-year 10-K available for a direct year-over-year comparison. A prior-year filing was not available for Salamander Innisbrook, LLC (1418372), INTERNATIONAL BATTERY METALS LTD. (1786318) and Piermont Valley Acquisition Corp (1865248), so they are excluded from the ranking.
SEC What Changed Methodology
Each company is scored on how similar its current annual filing text is to the prior year. Scores run from 0 to 1 — a score of 1 means the language is essentially unchanged; a lower score means more has changed. We flag three sections that carry the most disclosure signal: Business, Risk Factors, and MD&A. Recent research suggests that lower scores indicate that a company has made significant changes to their filings, these changes are often buried in the filings. If a company was to report positive news, they would likely do so in the form of a press release or statement on their website. The large changers have often underperformed in the market, while the stable-language filers have earned positive abnormal returns.
Key Takeaways
- Grace Therapeutics, Inc. (Medium) — The key change is that Grace Therapeutics now frames GTx-104 around an FDA CRL and resubmission process, making regulatory timing the main near-term risk.
- Jerash Holdings (US), Inc. (Medium) — Jerash is still leaning into capacity expansion, and the new factory purchase makes future growth more tangible but also more dependent on demand staying strong.
- Earth Science Tech, Inc. (Medium) — The key change is a clearer push to sell Earth Science Tech as a vertically integrated healthcare and consumer platform, but the business remains fragmented and microcap trading risk is still front and center.
- AMERICAN HONDA FINANCE CORP (Medium) — The key change is a clearer warning that tariffs and Honda’s broader strategic relationships could now weigh more on AHFC’s financing and credit outlook.
- Medtronic plc (High) — Medtronic is signaling a more focused, tech-driven strategy while moving to spin off Diabetes, a change that could materially reshape the company’s growth and margin story.
- Central Plains Bancshares, Inc. (Medium) — The key change is a clearer warning that cyber, vendor, and portfolio-quality issues could now have a more visible impact on results.
Ranking Table
| Rank | Company | CIK | Full Filing Similarity | Business Similarity | Risk Factors Similarity | MD&A Similarity | Most Changed Section | Assessment |
|---|---|---|---|---|---|---|---|---|
| 1 | Grace Therapeutics, Inc. | 1444192 | 0.871 | 0.999 | 0.999 | 0.999 | Business | medium |
| 2 | Jerash Holdings (US), Inc. | 1696558 | 0.994 | 0.929 | 0.996 | 0.996 | Business | medium |
| 3 | Earth Science Tech, Inc. | 1538495 | 0.98 | 0.936 | 0.983 | 0.987 | Business | medium |
| 4 | AMERICAN HONDA FINANCE CORP | 864270 | 0.995 | 0.977 | 1 | 0.999 | Business | medium |
| 5 | Medtronic plc | 1613103 | 0.99 | 0.996 | 0.982 | 0.998 | Risk Factors | high |
| 6 | Central Plains Bancshares, Inc. | 1979332 | 0.993 | 1 | 0.998 | 0.998 | Risk Factors | medium |
Grace Therapeutics, Inc. (1444192)
| Rank | 1 |
|---|---|
| Lowest similarity section | Business |
| Assessment | medium |
| SEC filings | 2026 10-K HTML/iXBRL (SEC page, raw text) | 2025 10-K HTML/iXBRL (SEC page, raw text) |
Grace Therapeutics’ 10-K shows a bigger intellectual property portfolio and a continued focus on reformulating approved drugs for rare diseases through the 505(b)(2) route. The most important new disclosure is that GTx-104 is now tied to a Complete Response Letter and a planned FDA Type A meeting, which makes the regulatory path more explicit and more uncertain. The company also completed its move to Delaware and adopted its new name.
Main Changes
- The company says its pipeline is now supported by “more than 79 granted and pending patents,” up from “more than 40” patents previously, signaling a larger intellectual property base around its rare-disease programs.
- The business description now says the company seeks to use proprietary formulations to improve efficacy, onset, side effects, convenience and compliance, while emphasizing the Section 505(b)(2) pathway as a “potentially shorter path to regulatory approval.”
- The filing adds that the company completed a continuance and domestication into Delaware and changed its name to Grace Therapeutics, Inc., with its subsidiary renamed Grace Therapeutics U.S., Inc.
- The risk discussion now specifically highlights GTx-104’s Complete Response Letter, a scheduled Type A meeting with FDA, and the need to resubmit the NDA, replacing the prior more general approval-timing language.
Watch Items
- A larger patent count can strengthen exclusivity and partnering leverage, which matters for a small biotech trying to protect future product value.
- The explicit CRL and resubmission language shows GTx-104 remains the key regulatory catalyst and that approval timing is still uncertain.
- The Delaware redomestication and name change are corporate housekeeping, but they also mark a cleaner U.S.-centric structure for future financing or strategic transactions.
Important Filing Changes
We aim to effectively treat debilitating symptoms that result from these underlying diseases. Our management team possesses significant experience in drug formulation, drug delivery research and development, clinical and pharmaceutical development, manufacturing, regulatory affairs, business development, as well as late-stage drug development and commercialization. Importantly, our team is comprised of industry professionals with deep expertise and knowledge, including a world-renowned practicing neurosurgeon-scientist and respected authority in aneurysmal subarachnoid hemorrhage, as well as product development, chemistry, manufacturing and controls (“CMC”), planning, implementation, management, and execution of global Phase 2 and Phase 3 trials for GTx-104, and drug commercialization.
We aim to effectively treat debilitating symptoms that result from these underlying diseases. Our management team possesses significant experience in drug formulation, drug delivery research and development, manufacturing, regulatory affairs, business development, as well as late-stage drug development and commercialization. Importantly, our team is comprised of industry professionals with deep expertise and knowledge, including a world-renowned practicing neurosurgeon-scientist and respected authority in aneurysmal subarachnoid hemorrhage, as well as product development, chemistry, manufacturing and controls (“CMC”), planning, implementation, management, and drug commercialization.
Our management team possesses significant experience in drug formulation, drug delivery research and development, clinical and pharmaceutical development, manufacturing, regulatory affairs, business development, as well as late-stage drug development and commercialization. Importantly, our team is comprised of industry professionals with deep expertise and knowledge, including a world-renowned practicing neurosurgeon-scientist and respected authority in aneurysmal subarachnoid hemorrhage, as well as product development, chemistry, manufacturing and controls (“CMC”), planning, implementation, management, and execution of global Phase 2 and Phase 3 trials for GTx-104, and drug commercialization. Our Pipeline • GTx-104 is a clinical stage, novel, injectable formulation of nimodipine being developed for IV infusion in aSAH patients to address significant unmet medical needs.
Our management team possesses significant experience in drug formulation, drug delivery research and development, manufacturing, regulatory affairs, business development, as well as late-stage drug development and commercialization. Importantly, our team is comprised of industry professionals with deep expertise and knowledge, including a world-renowned practicing neurosurgeon-scientist and respected authority in aneurysmal subarachnoid hemorrhage, as well as product development, chemistry, manufacturing and controls (“CMC”), planning, implementation, management, and drug commercialization. The unique nanoparticle technology of GTx-104 facilitates aqueous formulation of insoluble nimodipine for a standard peripheral IV infusion.
Risk Factors Risks Factors Relating to our Business We may not achieve our publicly announced milestones on time, or at all. From time to time, we may publicly announce the timing of certain events that we expect to occur, such as the anticipated timing of upcoming new drug application filing.
Risk Factors Risks Factors Relating to our Business We received a Complete Response Letter (CRL) from the FDA citing certain manufacturing deficiencies and other non-clinical issues, which may delay or prevent approval of GTx-104. In April 2026, we received a CRL from the FDA in response to our NDA for GTx-104.
Jerash Holdings (US), Inc. (1696558)
| Rank | 2 |
|---|---|
| Lowest similarity section | Business |
| Assessment | medium |
| SEC filings | 2026 10-K HTML/iXBRL (SEC page, raw text) | 2025 10-K HTML/iXBRL (SEC page, raw text) |
Jerash’s business description shows a company still adding manufacturing capacity and worker housing, but with more specific timing and asset details than before. The biggest new item is the completed purchase of Property No. 1326, which is expected to become the sixth factory and start production in fiscal 2027. The filing also updates the China lease and confirms the housing project was finished in fiscal 2025.
Main Changes
- The company updated its housing project from a 189,000-square-foot facility to a 195,000-square-foot facility and said construction was completed in fiscal 2025, with workers now moved in.
- Jerash replaced the prior reference to a planned seventh factory with a more concrete expansion plan, saying it is finalizing design work for a new project on a 133,000-square-foot parcel and that 2/3 of the land will be used for a seventh factory.
- The China lease disclosure was refreshed to say Jiangmen Treasure Success entered a new five-year lease on January 1, 2026, with monthly rent of CNY66,353 and 3% annual increases starting in year two.
- The business section added that Jerash received approval on February 2, 2026 to buy Property No. 1326 in South Amman, completed the purchase on February 19, 2026, and expects it to become the sixth factory with production starting in fiscal 2027.
Watch Items
- The new property purchase and planned sixth factory signal continued capacity expansion, which could support revenue growth if customer demand holds up.
- The updated lease terms and higher rent on the China facility modestly raise fixed-cost exposure and make utilization more important.
- Management’s willingness to keep investing in housing and factories suggests confidence in long-term demand, but execution now depends on order flow and business development.
Important Filing Changes
Business—Organizational Structure.” In 2018, we commenced another project to build a 54,000 square-foot factory in Al-Hasa County in the Tafilah Governorate of Jordan, which started operation in November 2019. This project is a joint project with the Jordanian Ministry of Labor and the Employment and Training Department in Jordan.
Business—Organizational Structure.” In 2018, we commenced a project to build a 54,000 square-foot factory in Al-Hasa County in the Tafilah Governorate of Jordan, which started operation in November 2019. This project is a joint project with the Jordanian Ministry of Labor and the Employment and Training Department in Jordan.
In April 2021, we commenced construction on a 189,000-square-foot housing facility for our multi-national workforce, situated on a 49,000-square-foot site owned by us, located in Al Tajamouat Industrial City. The construction has been completed as of the date of this annual report and our workers have started moving in. To meet increasing demand, we are also finalizing plans to construct an additional project on a nearby 133,000-square-foot parcel that we purchased in 2019 for $1.2 million, with 2/3 of the land expected to be allocated for the establishment of our seventh factory and 1/3 for housing purposes.
In April 2021, we commenced construction on a 195,000-square-foot housing facility for our multi-national workforce, situated on a 49,000-square-foot site owned by us, located in Al Tajamouat Industrial City. In fiscal 2025, the construction completed and our workers have moved in. To meet increasing demand, we are also finalizing plans to construct an additional project on a nearby 133,000-square-foot parcel that we purchased in 2019 for $1.2 million, with 2/3 of the land expected to be allocated for the establishment of our seventh factory and 1/3 for housing purposes.
The following discussion of our financial condition and results of operations should be read in conjunction with our consolidated financial statements and the related notes included elsewhere in this annual report. Executive Overview Seasonality of Sales A significant portion of our revenue is received during the first six months of our fiscal year. The majority of our VF Corporation orders are derived from winter season fashions, the sales of which occur in Spring and Summer and are merchandized by VF Corporation during the months of September through November.
The following discussion of our financial condition and results of operations should be read in conjunction with our consolidated financial statements and the related notes included elsewhere in this annual report. Executive Overview Seasonality of Sales We used to have strong seasonality due to higher values of fall and winter orders, which are normally shipped in the first two quarters of our fiscal years. We have been working on smoothing out seasonality through expansions of customer base and product offerings.
Earth Science Tech, Inc. (1538495)
| Rank | 3 |
|---|---|
| Lowest similarity section | Business |
| Assessment | medium |
| SEC filings | 2026 10-K HTML/iXBRL (SEC page, raw text) | 2025 10-K HTML/iXBRL (SEC page, raw text) |
Earth Science Tech’s filing gives a more expansive and more integrated description of the business, especially in healthcare, where it now highlights the link between telehealth and proprietary pharmacy fulfillment. It also recasts the real estate arm as an internal asset-management function and gives MagneChef a more technology-driven consumer pitch. The risk section is largely the same, aside from updating the trading venue from OTC Pink to OTCID.
Main Changes
- The Business section now says the company competes across "pharmaceutical compounding, telemedicine, clinical wellness, real estate asset management, and direct-to-consumer goods," expanding the description from a narrower set of segments.
- It adds that the company’s edge is its "unique vertical integration," linking "clinical consultation with our proprietary pharmacy fulfillment" to deliver a "value added healthcare experience" and "higher quality control."
- The real estate unit is reframed from a standalone business to a foundation for "managing the Company’s assets," while MagneChef is positioned around "proprietary magnetic heat-conduction technology" and "digital-first performance marketing."
- The stock trading risk now says the common stock is quoted on the "OTCID Marketplace" instead of the "OTC Pink Marketplace."
Watch Items
- The new emphasis on vertical integration suggests management wants investors to view the company as a connected healthcare platform rather than a collection of unrelated businesses.
- The OTCID reference may matter for liquidity and market perception, since venue changes can affect how thinly traded microcap shares are viewed by investors.
- The stronger product and technology framing for MagneChef implies the company is trying to sharpen its consumer brand story, but execution risk remains high across multiple segments.
Important Filing Changes
BUSINESS BUSINESS BACKGROUND AND OVERVIEW Earth Science Tech, Inc. (“ETST” or the “Company”) was incorporated under the laws of the State of Nevada on April 23, 2010, and subsequently redomiciled to the State of Florida on June 27, 2022. As of November 8, 2022, ETST operates as a strategic holding company, focused on value creation through the acquisition, operational optimization, and management of its operating businesses.
BUSINESS BUSINESS BACKGROUND AND OVERVIEW Earth Science Tech, Inc. (“ETST” or the “Company”) was incorporated under the laws of the State of Nevada on April 23, 2010, and subsequently redomiciled to the State of Florida on June 27, 2022, headquartered in Miami, Florida. ETST operates as a diversified holding company focused on the health and wellness sector.
BUSINESS BUSINESS BACKGROUND AND OVERVIEW Earth Science Tech, Inc. (“ETST” or the “Company”) was incorporated under the laws of the State of Nevada on April 23, 2010, and subsequently redomiciled to the State of Florida on June 27, 2022. As of November 8, 2022, ETST operates as a strategic holding company, focused on value creation through the acquisition, operational optimization, and management of its operating businesses. The Company’s current operations include compounding pharmaceuticals, telemedicine and real estate development through its wholly owned subsidiaries: RxCompoundStore.com, LLC (“RxCompound”), Peaks Curative, LLC (“Peaks”), Avenvi, LLC (“Avenvi”), Mister Meds, LLC (“Mister Meds”), and Earth Science Foundation, Inc. (“ESF”).
BUSINESS BUSINESS BACKGROUND AND OVERVIEW Earth Science Tech, Inc. (“ETST” or the “Company”) was incorporated under the laws of the State of Nevada on April 23, 2010, and subsequently redomiciled to the State of Florida on June 27, 2022, headquartered in Miami, Florida. ETST operates as a diversified holding company focused on the health and wellness sector. The Company’s principal operating strategy is to build a vertically integrated healthcare platform that combines compounding pharmacy operations, telemedicine platforms, clinical support, and patient fulfillment.
We rely heavily on brand strength to differentiate ourselves in the market. If we fail to effectively promote, protect, or maintain our brand, our reputation could suffer, negatively impacting customer acquisition, retention, and partnership opportunities. If our offerings fail to achieve or maintain market acceptance, our financial performance could be adversely affected.
See “Cautionary Note Regarding Forward-Looking Statements.” Summary of Principal Risk Factors ● Our results of operations, as well as our key metrics, may fluctuate on a quarterly and annual basis, which may result in our failing to meet the expectations of industry and securities analysts or our investors. ● If we are unable to expand the scope of our offerings, including the number and type of products and services that we offer, the number and quality of healthcare providers serving our customers, and the number and types of conditions capable of being treated through our platform, our business, financial condition, and results of operations may be materially and adversely affected. ● If we are unable to successfully market to new customers and retain existing customers, or if evolving privacy, healthcare, or other laws prevent or limit our marketing activities, our business, financial condition, and results of operations could be harmed. ● We operate in highly competitive markets and face competition from large, well-established healthcare providers and more traditional retailers and pharmaceutical providers with significant resources, and, as a result, we may not be able to compete effectively. ● Our brand is integral to our success. If we fail to effectively maintain, promote, and enhance our brand in a cost-effective manner, our business and competitive advantage may be harmed. 9 ● Our pharmacy business subjects us to additional healthcare laws and regulations beyond those we face with our telehealth business and increases the complexity and extent of our compliance and regulatory obligations. ● If we fail to comply with applicable healthcare and other governmental regulations, we could face substantial penalties, in which case our business, financial condition, and results of operations could be adversely affected, and we may be required to restructure our operations. ● Evolving government regulations and enforcement activities may require increased costs or adversely affect our results of operations. ● Security breaches, loss of data, and other disruptions could compromise sensitive information related to our business or customers or prevent us from accessing critical information and expose us to liability, which could adversely affect our business and our reputation. ● We may be subject to legal proceedings and litigation, including intellectual property disputes, which are costly to defend and could materially harm our business and results of operations. ● We may require additional capital to support business growth, and this capital might not be available on acceptable terms, if at all. ● Our Series B class Preferred stock structure has the effect of concentrating voting power with our Chief Executive Officer and Chairman of the Board, Giorgio R.
AMERICAN HONDA FINANCE CORP (864270)
| Rank | 4 |
|---|---|
| Lowest similarity section | Business |
| Assessment | medium |
| SEC filings | 2026 10-K HTML/iXBRL (SEC page, raw text) | 2025 10-K HTML/iXBRL (SEC page, raw text) |
American Honda Finance expanded its risk disclosure to call out tariffs and Honda’s business alliances and joint ventures as specific concerns. It also updated balance-sheet and cash requirement figures, showing higher debt and higher subsidiary liabilities than last year. The operating assumptions in MD&A were refreshed, with slightly higher downside sensitivity on credit losses and lease residual values.
Main Changes
- The forward-looking risk list now adds "risks with Honda Motor Co., Ltd.’s current business alliances and joint ventures and any future potential business alliances, joint ventures, or business combinations."
- It also adds a new tariff-specific risk: "the impact of tariffs enacted, proposed, revised, or suspended by governments applicable to the automotive industry" and possible retaliatory measures.
- The macro risk wording was broadened from "changes in economic and general business conditions" to include "changes in exchange rates" and more explicit trade-policy uncertainty.
- The Business section updated debt and liquidity figures, with outstanding indebtedness rising to $73.5 billion from $71.3 billion and subsidiary liabilities increasing to $22.6 billion from $19.2 billion.
Watch Items
- The new tariff and alliance language suggests management sees Honda’s auto ecosystem as more exposed to policy and strategic-partnership risk than before.
- Higher debt and subsidiary liabilities point to a larger balance-sheet footprint, which matters for funding flexibility and credit monitoring.
- The updated lease and credit-loss sensitivities show somewhat higher downside exposure if used-vehicle values or unemployment worsen.
Important Filing Changes
Material Cash Requirements The following table summarizes our material cash requirements from contractual obligations, excluding lending commitments to dealers and derivative obligations, by fiscal year payment period, as of March 31, 2025: Payments due by period Total 2026 2027 2028 2029 2030 Thereafter (U.S. dollars in millions) Unsecured debt obligations (1) $ 50,293 $ 19,132 $ 9,866 $ 7,385 $ 5,503 $ 1,754 $ 6,653 Secured debt obligations (1) 12,402 6,289 3,981 1,874 258 — — Interest payments on debt (2) 5,673 2,009 1,290 861 548 352 613 Total $ 68,368 $ 27,430 $ 15,137 $ 10,120 $ 6,309 $ 2,106 $ 7,266 _______________________ (1) Debt obligations reflect the remaining principal obligations of our outstanding debt and do not reflect unamortized debt discounts and fees. Repayment schedule of secured debt reflects payment performance assumptions on underlying receivables. Foreign currency denominated…
Material Cash Requirements The following table summarizes our material cash requirements from contractual obligations, excluding lending commitments to dealers and derivative obligations, by fiscal year payment period, as of March 31, 2026: Payments due by period Total 2027 2028 2029 2030 2031 Thereafter (U.S. dollars in millions) Unsecured debt obligations (1) $ 49,548 $ 15,984 $ 10,909 $ 8,579 $ 2,130 $ 5,289 $ 6,657 Secured debt obligations (1) 15,367 8,013 4,911 2,172 271 — — Interest payments on debt (2) 6,151 2,152 1,439 932 589 480 559 Total $ 71,066 $ 26,149 $ 17,259 $ 11,683 $ 2,990 $ 5,769 $ 7,216 _______________________ (1) Debt obligations reflect the remaining principal obligations of our outstanding debt and do not reflect unamortized debt discounts and fees. Projected repayment schedule of secured debt reflects payment performance assumptions on underlying assets. Foreign currency-denominated debt principal is based on exchange rates as of March 31, 2026. (2) Interest payments on floating rate and foreign currency-denominated debt based on the applicable floating rates and/or exchange rates as of March 31, 2026.
Refer to Note 5—Derivative Instruments of Notes to Consolidated Financial Statements for additional information on derivative instruments. 39 Derivatives We utilize derivative instruments to mitigate exposures to fluctuations in interest rates and foreign currency exchange rates. The types of derivative instruments include interest rate swaps, basis swaps, and cross currency swaps.
Refer to Note 5—Derivative Instruments of Notes to Consolidated Financial Statements for additional information on derivative instruments. 41 Derivatives We utilize derivative instruments to manage exposures to interest rate and foreign currency risks. Our assets consist primarily of fixed rate receivables and operating lease assets.
Medtronic plc (1613103)
| Rank | 5 |
|---|---|
| Lowest similarity section | Risk Factors |
| Assessment | high |
| SEC filings | 2026 10-K HTML/iXBRL (SEC page, raw text) | 2025 10-K HTML/iXBRL (SEC page, raw text) |
Medtronic’s filing shows a more explicit push toward AI, automation, and connected care, alongside a significant plan to separate the Diabetes business into MiniMed. The company also broadened its risk discussion to reflect faster technology change, more legal and data-privacy exposure, and tougher reimbursement pressure. Overall, the filing reads like a strategic reset toward a leaner portfolio and more digitally enabled growth.
Main Changes
- The Business section now says Medtronic is "evolving our business strategy in three key areas," adding a new emphasis on "turn data, artificial intelligence (AI), and automation into action" to tailor therapies, support remote monitoring, and create new standards of care.
- Medtronic added a major portfolio change: in May 2025 it announced plans to separate the Diabetes business into a new public company, MiniMed Group, Inc., and says MiniMed completed an IPO on March 9, 2026.
- The risk-factor summary was broadened to include "rapid technological change," "intellectual property protection and enforcement," "litigation, claims, and investigations," and "cybersecurity and data privacy incidents," while also expanding supply-chain language to cover "manufacturing operations."
- The reimbursement language was tightened to note more pressure from "lower-cost sites of service" and "utilization management programs (e.g., prior authorization)," signaling a more challenging pricing environment.
Watch Items
- The Diabetes separation is a meaningful portfolio reshaping that could change Medtronic’s growth profile, margin mix, and capital allocation priorities.
- The new AI and automation language suggests management is leaning harder into digital and connected-care products, which could support differentiation if execution is strong.
- Expanded risk disclosures around IP, investigations, and data privacy point to a broader operating-risk backdrop that investors should monitor for legal or compliance costs.
Important Filing Changes
The Audit Committee discusses policies with respect to risk assessment and risk management, including risks associated with the reliability and security of the Company’s information technology and security systems, and the steps management has undertaken to monitor and control such exposures. The Audit Committee receives regular updates on the Company’s cybersecurity risk management program from the CISO and CIO, and our procedures specify escalation of certain cybersecurity events to the Audit Committee chair and full Audit Committee. Cybersecurity Risk Board Committee or Subcommittee Responsible for Oversight [Text Block] The cybersecurity risk management program is led by the Chief Information Security Officer (CISO).
The ERM program establishes a risk management framework that seeks to identify, assess, and mitigate risks that could materially impact the Company’s business and operation. We engage third-party service providers, such as consultants and independent auditors, to support elements of our cybersecurity and risk management program. These engagements are overseen by cybersecurity leadership and results are incorporated into our ongoing risk management and continuous improvement efforts.
In addition, given the smart technology within our devices, our product security includes design protocols and is supported by quality systems testing and use scanning tools to assess and detect vulnerabilities that could affect our products. Risks from cybersecurity threats are integrated into Medtronic’s enterprise risk management (ERM) program. The ERM program establishes a risk management framework that seeks to identify, assess, and mitigate risks that could materially impact the Company’s business and operation.
We engage third-party service providers, such as consultants and independent auditors, to support elements of our cybersecurity and risk management program. These engagements are overseen by cybersecurity leadership and results are incorporated into our ongoing risk management and continuous improvement efforts. We maintain a third-party risk management process designed to identify and manage cybersecurity risks associated with key third-party relationships.
Patients around the world deserve access to our life-saving products, and we are driven to use our local presence and scale to increase the adoption of our products and services in markets around the globe. • Deliver superior outcomes and better experiences for patients and providers: We listen to our patients and customers to better understand the challenges they face. From the patient journey, to creating agile partnerships that produce novel solutions, to making it easier for our customers to deploy our therapies — what we do is anchored in deep insight, and creates simpler, superior experiences. • Turn data, artificial intelligence (AI), and automation into action: We are confident in our ability to maximize new technology, AI, and data and analytics to tailor therapies in real-time, facilitating remote monitoring and care delivery that conveniently manages conditions, and creates new…
Patients around the world deserve access to our life-saving products, and we are driven to use our local presence and scale to increase the adoption of our products and services in markets around the globe. • Deliver superior outcomes and better experiences for patients and providers: We listen to our patients and customers to better understand the challenges they face. From the patient journey, to creating agile partnerships that produce novel solutions, to making it easier for our customers to deploy our therapies — what we do is anchored in deep insight, and creates simpler, superior experiences. • Turn data, AI, and automation into action: We are confident in our ability to maximize new technology, AI, and data and analytics to tailor therapies in real-time, facilitating remote monitoring and care delivery that conveniently manages conditions, and creates new standards of care. We have three reportable segments that primarily develop, manufacture, distribute, and sell device-based medical therapies and services: the Cardiovascular Portfolio, the Neuroscience Portfolio, and the Medical Surgical Portfolio.
Central Plains Bancshares, Inc. (1979332)
| Rank | 6 |
|---|---|
| Lowest similarity section | Risk Factors |
| Assessment | medium |
| SEC filings | 2026 10-K HTML/iXBRL (SEC page, raw text) | 2025 10-K HTML/iXBRL (SEC page, raw text) |
Central Plains Bancshares expanded its risk disclosures to cover technology disruption, vendor dependence, and cyber/security failures. It also added a broader warning about changes in the quality or mix of its loan and investment portfolios. The update reads like a more explicit acknowledgment that operational and balance-sheet risks are important for a small community bank.
Main Changes
- The risk factor list now explicitly adds "technological changes that may be more difficult or expensive than expected" and "the inability of third-party providers to perform as expected."
- A new risk was added for "a failure or breach of our operational or information security systems," expanding the company’s disclosure around cyber and systems disruption.
- The filing also adds a new risk tied to changes in the "quality or composition of our loan or investment portfolios," which broadens the credit and balance-sheet risk discussion.
Watch Items
- The added cyber and vendor language suggests management sees operational resilience as a more important risk, which can imply higher compliance and security spending.
- New third-party provider risk matters because smaller banks often rely on outside vendors for core processing, digital banking, and other critical services.
- The portfolio-quality language signals more sensitivity to asset mix and credit performance, which investors should watch for in future loan and investment trends.
Important Filing Changes
At March 31, 2025, we had consolidated assets of $508.7 million, consolidated deposits of $416.2 million and consolidated stockholders’ equity of $83.3 million. Our executive offices are located at principal office is located at 221 South Locust Street, Grand Island, Nebraska 68801, and our telephone number at that address is (308) 382-4000. Home Federal Savings Originally chartered in 1935, Home Federal Savings, which operates under the name “Home Federal Bank,” is a federally-chartered stock savings association headquartered in Grand Island, Nebraska.
At March 31, 2026, we had consolidated assets of $558.6 million, consolidated deposits of $460.4 million and consolidated stockholders’ equity of $89.0 million. Our principal executive offices are located at 221 South Locust Street, Grand Island, Nebraska 68801, where our main administrative functions are conducted. Our telephone number at that address is (308) 382-4000.
Home Federal Savings Originally chartered in 1935, Home Federal Savings, which operates under the name “Home Federal Bank,” is a federally-chartered stock savings association headquartered in Grand Island, Nebraska. Our main office is located at 221 South Locust Street, Grand Island, Nebraska 68801, and our telephone number at that address is (308) 382-4000. Our website address is www.homefederalne.bank .
Our principal executive offices are located at 221 South Locust Street, Grand Island, Nebraska 68801, where our main administrative functions are conducted. Our telephone number at that address is (308) 382-4000. Home Federal Savings Originally chartered in 1935, Home Federal Savings, which operates under the name “Home Federal Bank,” is a federally-chartered stock savings association headquartered in Grand Island, Nebraska.
001-41844), filed with the SEC on June 21, 2024). Kunzman (incorporated by reference to Exhibit 10.1 to the Current Report on Form 8-K of the Company (file no. 001-41844), filed with the SEC on October 26, 2023).
333-283501), filed with the SEC on November 27, 2024) 10.8 Employment Agreement with Dannel R. Garness (incorporated by reference to Exhibit 10.8 to the Annual Report on Form 10-K of the Company (files no. 001-41844), filed with the SEC on June 26, 2026).
Why SEC Filing Changes Matter
Research by Cohen et al. (Lazy Prices, 2020) — using the complete history of SEC filings from 1995 to 2014 — shows that when firms make active changes to their annual disclosures, those changes convey an important signal about future operations and returns. A portfolio that shorted "changers" and bought "non-changers" earned over 22% per year in annual alpha historically. Changes to the Risk Factors section, Business description, and language referring to the executive team were especially informative. Critically, these returns accrued gradually as information was later revealed through news and earnings — not at the time of filing — suggesting many investors remain inattentive to these simple, public signals. This snapshot is a starting point for deeper investigation, not a buy or sell recommendation.
For more like this, see the full SEC What Changed archive, browse more equity research reports, or subscribe to Quantitative Research Notes for new filing-change alerts as soon as they publish.
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