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PODDInsulet Corporation

Health care · Medical Instruments · Nasdaq
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The 10-K against last year's

182 changes: 31 added, 50 removed, 97 reworded, 4 quiet changes

10-K Feb 18, 2026 vs Feb 21, 2025
Risk FactorsRedline ↓
27.7%
of the text changed · 9,410 words now
44.4%
of the text changed · 5,503 words now
Legal ProceedingsRedline ↓
90.1%
of the text changed · 486 words now
Accounting PoliciesRedline ↓
13.5%
of the text changed · 4,373 words now

10-K 0001145197-26-000028 (2026-02-18) vs 10-K 0001145197-25-000007 (2025-02-21)

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.

Legal Proceedings New paragraph this year (276 words), with no similar paragraph last year.
On April 24, 2025, the United States District Court for the District of Massachusetts entered final judgment in favor of Insulet Corporation in its ongoing litigation against EOFlow Co., Ltd.; EOFlow, Inc.; Nephria Bio, Inc.; and EOFlow’s CEO, Jesse Kim (collectively, “Defendants”), Insulet Corp. v. EOFlow Co. Ltd. et al., 1:23-cv-11780-FDS (D. Mass.). The litigation concerned the Defendants’ misappropriation of Insulet’s proprietary trade secrets relating to the design and manufacture of the Omnipod insulin patch pump. On December 3, 2024, a unanimous jury found four trade secrets asserted by Insulet valid and misappropriated and awarded Insulet total damages of $452 million, composed of $170 million in compensatory damages and $282 million in exemplary damages. The district court’s April 24, 2025 orders upheld the jury verdict and further entered a permanent injunction against Defendants. The injunction prohibits Defendants and others subject to the order from using, possessing, selling, distributing, or seeking regulatory approval for any products that were designed, developed, or manufactured, in whole or in part, using or relying on Insulet’s trade secrets. The injunction is worldwide and took effect immediately subject to a limited exception that permits six months of continuing sales to those patients of EOFlow that existed in the Republic of Korea and the European Union as of October 2023. The permanent injunction further requires EOFlow to assign certain patent applications to Insulet, disgorge any break-up fees received from Medtronic in connection with a previously contemplated acquisition, and submit to ongoing audits to ensure compliance with the district court’s orders. In view of the scope of the permanent injunction, the Court reduced Insulet’s monetary award to $59.4 million to avoid a double recovery.

Source: Item 3, via Note 16 – Commitments and Contingencies, 10-K 0001145197-26-000028 vs Item 3, via Note 18 – Commitments and Contingencies, 10-K 0001145197-25-000007

MD&A 260 words changed in this paragraph; it is 40% similar to last year's version.
We exercise significant judgment generally recognize revenue when control of our products is transferred to customers in an amount that reflects the net consideration we determine variable consideration adjustments. As discussed in Note 2 expect to our consolidated financial statements, we receive. Our products are subject to pricing rebates on pricing programs under arrangements with managed care organizations, such as including pharmacy benefit managers, governmental payors, and third-party commercial payors, primarily in the United States. Reductions These rebates represent amounts owed pursuant to our revenues contractual agreements or legal requirements after the product is dispensed to a benefit plan participant. Provisions for rebates on products sold through our distributors under these rebates, collectively referred to as pharmacy benefits rebates, are treated as variable consideration and are recorded as a reduction to revenue using the most significant component of variable consideration. In addition, pharmacy rebates are most expected value method. Although we record a rebate provision at risk for significant adjustment because of the time delay between of sale, the recording of the provision when revenue is recognized and its ultimate settlement, an interval that related rebate payments are generally ranges from made 30 to 90 days, but can last days thereafter and, in certain cases, may extend up to one year. Our estimates for As a result of this timing difference, revenue recognized in a given period may include adjustments to rebate provisions recorded in prior periods. Estimates of pharmacy rebates are developed based on historical experience, revenue growth, sales trends, levels of inventory in the distribution channel lag, contract amendments channel, and trends. Pharmacy rebates contractual terms. A significant portion of our rebate provisions relate to sales of the Company’s products in the United States. United States pharmacy rebate provisions charged against gross sales amounted to $654.7 million, $452.7 million, and $367.3 million, and $175.2 million in 2025, 2024, and 2023, and 2022, respectively. When To the extent that actual pharmacy rebate settlements payments differ from our estimates, we adjust revise our estimates, which affects reported assumptions and record the resulting adjustments to revenue in the period that in which such variances differences become known.

Source: Item 7, 10-K 0001145197-26-000028 vs Item 7, 10-K 0001145197-25-000007

Risk Factors 217 words changed in this paragraph; it is 55% similar to last year's version.
As we continue to expand the number of customers we serve, driven in large part by significant increasing demand for Omnipod 5, our international expansion and entrance into the insulin-requiring type 2 diabetes market, we expect to continue to increase our manufacturing capacity, our personnel, and the scope of our sales and marketing efforts. This growth, as well as any other Our growth that we may experience in the future, will create challenges for our organization and may strain our management and operations resources, including our customer service. In order to manage future growth, we will be required to improve existing, and implement new, sales and marketing efforts, distribution channels, management, operations, and customer support procedures. In addition, the form and function of our enterprise information technology systems will need to change and be improved upon as our business needs change. For example, we recently implemented a new enterprise resource planning system and plan to upgrade our customer relationship management system. We will also need to manage our supply chain and manufacturing effectively, including our sourcing of materials such as semiconductor chips. We may also need to partner with additional third-party suppliers to manufacture certain components of our Omnipod products and install additional manufacturing lines, including as a part of our newly constructed facility in Malaysia. A transition to new suppliers may result in additional costs or delays. service resources. We may misjudge the amount of time or resources that will be required to effectively manage any anticipated or unanticipated growth in our business, or we may not be able to manufacture sufficient inventory, or and we may not be able to attract, hire, and retain sufficient personnel to meet our expanding needs. If we cannot scale our business appropriately, maintain control over expenses, manufacture our products in a cost-effective or timely manner, or otherwise adapt to anticipated and unanticipated growth, our business resources may become strained, customer experience may decline, and we may not be able to deliver our Omnipod products in a timely manner, and all of which would adversely affect our results of operations may be adversely affected. operations.

Source: Item 1A, 10-K 0001145197-26-000028 vs Item 1A, 10-K 0001145197-25-000007

Accounting Policies 101 words changed in this paragraph; it is 61% similar to last year's version.
The Company’s Drug Delivery product line includes sales of a modified version of the Pod to a pharmaceutical and biotechnology companies company who use the Company’s technology as a delivery method for their drugs. For the majority of this product line, revenue is recognized, with an associated unbilled receivable, as the The product is produced pursuant to the customer’s firm purchase commitments. The commitments, the Company has an enforceable right to payment for performance completed to date date, and the inventory has no alternative use to the Company. The Company recognizes Accordingly, revenue is recognized over time using a blend of percentage-of-completion method, measured based on costs incurred to date relative to total estimated costs at completion and time incurred to date relative to total production time to measure progress toward completion, which results in the satisfaction recognition of its performance obligations. The Company believes that both incurred cost and elapsed time reflect the value generated, which best depicts the transfer of control to the customer. Contract costs include third-party costs as well as an allocation of manufacturing overhead. associated unbilled receivable.

Source: Item 8, Note 2 – Summary of Significant Accounting Policies, 10-K 0001145197-26-000028 vs Item 8, Note 2 – Summary of Significant Accounting Policies, 10-K 0001145197-25-000007

Every change, by type

Sentences and paragraphs added, removed or reworded

Sentences and paragraphs of PODD's Risk Factors and MD&A, 10-K 2026-02-18 against 10-K 2025-02-21. Each links to the text at sec.gov.

RemovedRisk Factors
•development of an effective patch pump by one or more competitors or breakthrough diabetes treatments not requiring the delivery of insulin;

Read it in 10-K 2025-02-21 at sec.gov ↗

RemovedRisk Factors
•failure of our Omnipod products to achieve and maintain wide acceptance among opinion leaders in the diabetes treatment community, insulin-prescribing physicians, third-party payors, and people with insulin-dependent diabetes;

Read it in 10-K 2025-02-21 at sec.gov ↗

RemovedRisk Factors
If any of these events occur, our ability to generate revenue could be significantly reduced, which would adversely affect our business, financial condition, and results of operations.

Read it in 10-K 2025-02-21 at sec.gov ↗

Show the other 16
RemovedRisk Factors
reduced market acceptance and sales of our products, which would adversely affect our business, financial condition, and results of operations.

Read it in 10-K 2025-02-21 at sec.gov ↗

RemovedRisk Factors
In addition, some of our competitors, such as Medtronic, are large, well-capitalized companies with more resources than we have. These companies may have competitive advantages over us, including:

Read it in 10-K 2025-02-21 at sec.gov ↗

RemovedRisk Factors
•greater experience in conducting research and development, clinical trials, manufacturing, marketing, and obtaining regulatory approval; and

Read it in 10-K 2025-02-21 at sec.gov ↗

RemovedMD&A
In 2022, we issued two voluntary Medical Device Correction (“MDC”) notices, one for our Omnipod DASH PDM related to its battery and the other for our Omnipod 5 Controller related to its charging port and cable. During 2022, we initially recorded a net charge of $57.9 million related to these MDCs and, in 2023, we recorded $11.5 million of income associated with a change in our estimated liability for the MDCs, primarily due to lower distribution costs.

Read it in 10-K 2025-02-21 at sec.gov ↗

RemovedMD&A
Revenue from the sale of Omnipod products in the U.S. increased $258.3 million, or 20.6%, in 2024 to $1,509.3 million, compared with $1,251.0 million in 2023. This increase primarily resulted from higher volume through the pharmacy channel driven by growing our customer base, partially offset by a decrease in estimated inventory days-on-hand at distributors and lower conversions to Omnipod 5. Inventory days-on-hand declined to more normal levels following an acceleration of orders by U.S. pharmacy wholesales in advance of the implementation of our new ERP system on January 1, 2024. We experienced a benefit from conversions to Omnipod 5 in the prior year following the launch of the product in the latter half of 2022 since users generally fill both their Omnipod 5 starter kit and their first month of refills simultaneously. Conversions to Omnipod 5 declined since the vast majority of U.S. conversions to Omnipod 5 occurred in 2023. To a lesser extent, the revenue increase was driven by a higher average selling price resulting from our annual wholesale acquisition cost increase implemented during the second quarter of 2024 and growth in the pharmacy channel.

Read it in 10-K 2025-02-21 at sec.gov ↗

RemovedMD&A
Omnipod 5. A higher average selling price for Omnipod 5 compared with Omnipod DASH and Classic Omnipod also contributed to the revenue increase, although to a lesser extent.

Read it in 10-K 2025-02-21 at sec.gov ↗

RemovedMD&A
We expect selling, general and administrative expenses to increase in 2025 compared with 2024 due to investments in our operating structure, primarily headcount additions, particularly in the areas of customer support, sales and information technology support, to facilitate continued growth globally. We also plan to make additional investments to support the Omnipod platform and to continue support the phased launch of Omnipod 5 in our existing international markets and prepare for expansion into new countries.

Read it in 10-K 2025-02-21 at sec.gov ↗

RemovedMD&A
In 2021, the Organization for Economic Co-operation and Development (“OECD”) and G20 international forum released the Model Global Anti-Base Erosion (GloBE) rules (“Model Rules”) under Pillar Two. These Model Rules set forth the common approach for a Global Minimum Tax at 15% for multinational enterprises with revenue greater than €750 million and is expected to be applicable to Insulet. Pillar Two has been adopted by the Council of the European Union for implementation by European Union member states by December 31, 2023, with effect for tax years beginning 2024. Similar directives under Pillar Two are already adopted or expected to be adopted by taxing authorities in other countries where Insulet has business operations, with widespread implementation of the Global Minimum Tax in 2024 and 2025. There was no impact on the consolidated financial statements for 2024. While we do not expect the Pillar Two Model Rules and related legislation to have a material impact on our consolidated financial statements for 2025, we continue to evaluate their potential impact on future years.

Read it in 10-K 2025-02-21 at sec.gov ↗

RemovedMD&A
(1) Represents net (income) expense resulting from estimated costs associated with the voluntary MDC notices issued in the fourth quarter of 2022 and adjustments to those costs, which is included in cost of revenue. Refer to Note 13 to our consolidated financial statements for additional information.

Read it in 10-K 2025-02-21 at sec.gov ↗

RemovedMD&A
To finance our operations and global expansion, we have periodically issued convertible senior notes, which are convertible into our common stock. As of December 31, 2024, the following Convertible Senior Notes were outstanding:

Read it in 10-K 2025-02-21 at sec.gov ↗

RemovedMD&A
Issuance Date Coupon Principal Outstanding Due Date Conversion Rate(1) Conversion Price (in millions) per Share of Common Stock September 2019 0.375% $800.0 September 2026 4.4105 $226.73

Read it in 10-K 2025-02-21 at sec.gov ↗

RemovedMD&A
In connection with the issuance of the Convertible Senior Notes, we purchased capped call options (“Capped Calls”) on our common stock. By entering into the Capped Calls, we expect to reduce the potential dilution to our common stock (or, in the event the conversion is settled in cash, to provide a source of cash to settle a portion of our cash payment obligation) if at the time of conversion our stock price exceeds the conversion price under the Convertible Senior Notes. The Capped Calls have an initial strike price of $335.90 per share and cover 3.5 million shares of our common stock.

Read it in 10-K 2025-02-21 at sec.gov ↗

RemovedMD&A
Acquisitions—In 2023, we paid Bigfoot Biomedical, Inc. $25.1 million, including transaction costs, to acquire patent assets related to pump-based AID technologies. We also paid a purchase price holdback of $3.0 million associated with our 2022 acquisition of substantially all the assets related to the manufacture and production of shape-memory alloy wire assemblies used in the production of our product from Dynalloy, Inc.

Read it in 10-K 2025-02-21 at sec.gov ↗

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