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DGXQuest Diagnostics

Health care · Medical Labs · NYSE
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The 10-K against last year's

32 changes: 3 added, 3 removed, 26 reworded

10-K Feb 26, 2026 vs Feb 20, 2025
Risk FactorsRedline ↓
10.0%
of the text changed · 9,033 words now
Legal ProceedingsRedline ↓
4.3%
of the text changed · 2,441 words now
Accounting PoliciesRedline ↓
7.8%
of the text changed · 4,329 words now

10-K 0001022079-26-000015 (2026-02-26) vs 10-K 0001022079-25-000044 (2025-02-20) Not compared: MD&A.

The redline

The paragraph that changed most in each section

Marked against last year's 10-K: cut words struck through, new words highlighted and underlined.

Risk Factors 255 words changed in this paragraph; it is 37% similar to last year's version.
The FDA's regulation of clinical laboratory testing is expected to impact industry practices and participants, new competitors may enter the industry, and competition may come in new forms. As of In May 6, 2024, the FDA announced it was phasing out its general enforcement discretion approach so that LDTs manufactured by a laboratory will would generally fall under the same enforcement approach as medical devices. A number of advanced tests we develop internally are offered as LDTs. Pursuant to However, in March 2025, a U.S. District Court set aside and vacated the FDA’s decision LDT rule and the FDA did not appeal the court’s decision. Accordingly, the FDA does not have the authority to remove enforcement discretion with regard regulate LDTs. However, it is the purvey of Congress to most LDTs performed by high complexity CLIA-certified laboratories like ours, all enact new laws or amendments to CLIA or the Food, Drug and significantly modified previously offered laboratory tests that do not benefit from continued enforcement discretion will have Cosmetic Act. If this were to comply with the FDCA over a four-year, five-stage process. Compliance with the FDCA includes, among other things, new quality system regulations and premarket authorization. One major area of the continued FDA enforcement discretion will apply to many tests that were offered for clinical use prior to May 6, 2024 and that do not afterwards undergo certain material modifications. The removal of enforcement discretion for LDTs could result in a revitalization and passage of legislation or other Congressional action. The current FDA policy to remove enforcement discretion and/or occur, any new legislation is expected to could have a significant impact on us and the clinical laboratory testing industry, including regulating industry. This new legislation could include the regulation of LDTs in new ways, a manner that is different than the prior LDT rule, while creating new avenues of opportunity and competition regarding in clinical laboratory testing. New competitors may enter the industry, and competition may come in new forms.

Source: Item 1A, 10-K 0001022079-26-000015 vs Item 1A, 10-K 0001022079-25-000044

Accounting Policies 71 words changed in this paragraph; it is 50% similar to last year's version.
In November 2023, September 2025, the FASB issued a new accounting standard which will require companies impacts internal-use software accounting by removing all references to disclose significant segment expenses software development project stages such that are regularly provided the guidance is neutral to the chief operating decision maker ("CODM"). different software development methods. The pronouncement is effective for annual filings for the year ended December 31, 2024 2028 and for interim periods within such year. The Company is currently evaluating the year ended December 31, 2025. The adoption impact of this standard did not have a material impact on the Company's results of operations, financial position or cash flows. standard.

Source: 10-K text, Note 2 – SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES, 10-K 0001022079-26-000015 vs 10-K text, Note 2 – SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES, 10-K 0001022079-25-000044

Legal Proceedings 61 words changed in this paragraph; it is 58% similar to last year's version.
The Company also received subpoenas from the U.S. Attorney for the District of New Jersey. Jersey (the “NJ USAO”). The subpoenas seek various records relating to the Company’s relationship with the New York Giants and adherence to certain company policies and federal laws. The Company is cooperating settled the matter with the investigation. NJ USAO and agreed to enter into a Corporate Integrity Agreement with the Office of Inspector General of the United States Department of Health and Human Services. The Company has also received several subpoenas from the New York Attorney General’s Office, and is in the process of responding to them.

Source: Item 3, via Note 18 – COMMITMENTS AND CONTINGENCIES, 10-K 0001022079-26-000015 vs Item 3, via Note 18 – COMMITMENTS AND CONTINGENCIES, 10-K 0001022079-25-000044

Every change, by type

Sentences and paragraphs added, removed or reworded

Sentences and paragraphs of DGX's Risk Factors and MD&A, 10-K 2026-02-26 against 10-K 2025-02-20. Each links to the text at sec.gov.

Quiet changes are sentences kept from last year with one to four words changed, at least one of them a hedge, a modal or a qualifier (may, could, will, not, significant, material…). A year or date rolling forward is not counted.

The full word listadverse, adversely, all, although, anticipate, anticipates, any, approximately, believe, believes, can, cannot, certain, could, expect, expects, generally, however, if, intend, intends, largely, likely, many, material, materially, may, might, most, must, never, no, not, possible, primarily, probable, should, significant, significantly, some, substantial, substantially, unlikely, will, would
AddedRisk Factors
threatened by the U.S. government, and the responses to those actions from other countries, may result in adverse impacts to the global economic environment, including the global financial and trading markets, which could have a negative impact on our results of operations and financial condition. These actions could also negatively impact our supply chain costs or availability of products we need to operate our business. The ongoing uncertainty with the current state of global trade policy magnifies these risks.

Read it in 10-K 2026-02-26 at sec.gov ↗

AddedRisk Factors
(p) Challenges, including the associated competitive pressures, with properly managing the development, implementation, oversight and use of AI.

Read it in 10-K 2026-02-26 at sec.gov ↗

RemovedRisk Factors
From time to time, the federal government has considered whether competitive bidding could be used to provide clinical testing services for Medicare beneficiaries while maintaining quality and access to care. Congress also periodically considers cost-saving initiatives, which have included coinsurance for clinical testing services, co-payments for clinical testing and further laboratory physician fee schedule reductions.

Read it in 10-K 2025-02-20 at sec.gov ↗

RemovedRisk Factors
payment and requiring preauthorization of certain testing. There are also an increasing number of patients enrolling in consumer driven products and high deductible plans that involve greater patient cost-sharing.

Read it in 10-K 2025-02-20 at sec.gov ↗

RemovedRisk Factors
operating results. The potential impact of new policies that may be implemented as a result of the new administration is currently uncertain.

Read it in 10-K 2025-02-20 at sec.gov ↗

RewordedRisk Factors
However, unfavorable labor environments, unionization activity, or activity (including in non-U.S. markets), a failure to comply with labor or employment laws or reputational considerations triggered by any of the risks described in this Report could result in, among other things, labor unrest, strikes, work stoppages, slowdowns by the affected workers, fines fines, penalties and penalties. a loss of employees.

Read it in 10-K 2026-02-26 at sec.gov ↗

RewordedRisk Factors
We have a broad range of stakeholders, including our stockholders, employees, customers, which include government entities, patients and communities we serve, some of whom increasingly focus on corporate responsibility considerations. considerations and many have different or conflicting expectations with respect to corporate responsibility and related matters.

Read it in 10-K 2026-02-26 at sec.gov ↗

Show the other 10
RewordedRisk Factors
Other steps taken to reduce utilization and reimbursement include requirements to obtain diagnosis codes (which can be inconsistent between health plans and government payers) to obtain payment, increased documentation requirements, limiting the allowable number of tests or ordering frequency, expanded prior authorization programs and otherwise increasing payment denials.

Read it in 10-K 2026-02-26 at sec.gov ↗

RewordedRisk Factors
(c) A decline in Uncertain and volatile economic conditions, including the impact of an inflationary environment. environment and changes in government policies, including related to trade.

Read it in 10-K 2026-02-26 at sec.gov ↗

RewordedRisk Factors
Congress reintroduced federal introduced legislation in 2023 (the Saving Access to Laboratory Services Act), 2025, the Results Act, which would reform PAMA and create a true market-based CLFS.

Read it in 10-K 2026-02-26 at sec.gov ↗

RewordedRisk Factors
Using AI successfully will require significant resources, including having the technical expertise required to develop, test and maintain AI-based testing services. services and continually developing the appropriate governance and oversight of our use of AI.

Read it in 10-K 2026-02-26 at sec.gov ↗

RewordedRisk Factors
(h) Failure to efficiently integrate acquired businesses businesses, integrate our business with our joint ventures, and to manage the costs related to any such integration, integration and implementation requirements, or to retain key technical, professional or management personnel.

Read it in 10-K 2026-02-26 at sec.gov ↗

RewordedRisk Factors
It is important that we continue to strengthen our efficiency efficiency, including through the use of technology and automation, to promote our competitive position and enable us to mitigate the impact on our profitability of steps taken by government payers and health insurers to reduce the utilization and reimbursement of diagnostic information services, and to partly offset pressures from the current an inflationary environment, including labor and benefit cost increases, and reimbursement pressures.

Read it in 10-K 2026-02-26 at sec.gov ↗

RewordedRisk Factors
Acquisitions are not all the same (e.g., asset acquisitions differ from acquisitions of equity interests); different acquisitions offer different risks. risks and require different levels of effort to obtain regulatory clearance.

Read it in 10-K 2026-02-26 at sec.gov ↗

RewordedRisk Factors
This technology, including generative AI, which is in its early stages of broader commercial implementation, presents a number of risks inherent in its use, including risks related to cybersecurity, privacy and data security and use practices. practices and our oversight of how we use AI.

Read it in 10-K 2026-02-26 at sec.gov ↗

RewordedRisk Factors
For example, in February 2025, connection with Project Nova, we committed to a multi-year project ("Project Nova") to modernize our "Order to Cash" business processes processes, including the related information technology infrastructure and underlying enabling technologies.

Read it in 10-K 2026-02-26 at sec.gov ↗

RewordedRisk Factors
The process of combining negotiating, completing and integrating acquisitions may be disruptive to our businesses (especially as transactions become increasingly complex) and may cause an interruption of, or a loss of momentum in, such businesses as a result of the following difficulties, among others:

Read it in 10-K 2026-02-26 at sec.gov ↗

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