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RMDResMed

Health care · Medical Instruments · NYSE, OTC

We are a global leader in digital health and cloud-connected medical devices. 10-K, Item 1

Employees
11,370
Headquarters
San Diego, CA
CEO
Michael J. Farrell
Next results
around Jan 28, 2027
Compare with peers → Embed

10-K 0000943819-26-000047 (2026-08-13) vs 10-K 0000943819-25-000035 (2025-08-08)

SectionCompared textWords nowChanged
Risk FactorsItem 1A20,024 21.5%
MD&AItem 77,273 19.0%
Legal ProceedingsItem 391 not compared
Accounting PoliciesItem 8 (note not found)0 not compared

The redline: what was cut and what was added

In each section, the paragraph that changed most, marked against last year's 10-K: cut words struck through, new words highlighted and underlined.

Risk Factors 328 words changed in this paragraph; it is 55% similar to last year's version.
system requirements of ISO 13485:2016. Although the FDA has stated that the We are subject to substantial regulation related to quality standards contained in ISO 13485:2016 are substantially similar applicable to those set forth in the QSR, our manufacturing and although our quality system is currently designed processes. Our failure to comply with ISO these standards in connection with our device certifications, it is unclear the extent to which this final rule, once effective, could impose additional or different regulatory requirements on us that could increase the costs of compliance or otherwise negatively affect our business. If we are unable to comply with QMSR, once effective, or with any other new or existing laws or regulations enforced by FDA or comparable regulatory authorities, we may be subject to enforcement action, which could have an adverse effect on our business, financial condition condition, or results of operations. The FDA regulates the approval, manufacturing, and sales and marketing of many of our products in the U.S. Significant government regulation also exists in Canada, Japan, Europe, Australia, China, and other countries in which we conduct business. In February 2026, the FDA implemented the Quality Management System Regulation (QMSR), which replaces the prior FDA Quality System Regulation in setting forth the current good manufacturing practice (cGMP) requirements for medical devices, and incorporates ISO 13485 into U.S. law. The QMSR introduces changes to documentation, terminology, and inspection approaches, including expanded FDA visibility into internal audit, supplier oversight, and management review activities. As a device manufacturer, we are required to register with the FDA and are subject to periodic inspection by the FDA for compliance with the FDA’s QMSR, requirements, which require manufacturers of medical devices to adhere to certain regulations, including testing, quality control and documentation procedures. It remains unclear the extent to which the QMSR may impose additional or different regulatory requirements on us. Compliance may require ongoing updates to our processes, systems, and training, and failure to maintain compliance could result in regulatory actions, product recalls, or delays in approvals, which could adversely affect our business, financial condition, and results of operations. In addition, the federal Medical Device Reporting regulations require us to provide information to the FDA whenever there is evidence that reasonably suggests that a device may have caused or contributed to a death or serious injury or, if a malfunction were to occur, could cause or contribute to a death or serious injury. Compliance with applicable regulatory requirements is subject to continual review and is rigorously monitored through periodic inspections by the FDA. In the European Union, we are required to maintain certain ISO certifications and comply with the Medical Device Regulation (MDR) in order to sell our products and must undergo periodic inspections by notified bodies to obtain and maintain these certifications. Failure to comply with current governmental regulations and quality assurance guidelines could lead to temporary manufacturing shutdowns, product recalls or related field actions, product shortages or delays in product manufacturing. Efficacy or safety concerns, an increase in trends of adverse events in the marketplace, and/or manufacturing quality issues with respect to our products could lead to product recalls or related field actions, withdrawals, and/or declining sales.

Source: Item 1A, 10-K 0000943819-26-000047 vs Item 1A, 10-K 0000943819-25-000035

MD&A 119 words changed in this paragraph; it is 65% similar to last year's version.
Total other income (loss), net for the year ended June 30, 2025 2026 was a loss income of $7.8 $33 million, compared to a loss of $55.1 $8 million for the year ended June 30, 2024. 2025. We recorded interest income, net, of $4.1 $50 million for the year ended June 30, 2026 compared to interest income, net, of $4 million for the year ended June 30, 2025 compared to interest expense, net of $45.7 million for the year ended June 30, 2024 due to lower debt levels following the repayment of our revolving credit facility facility, gains recognized on cross-currency swaps associated with our fair value and net investment hedges, and interest earned on cash balances. Losses associated with our investments in marketable and non-marketable equity securities were $10.3 million for the year ended June 30, 2025 compared to a loss of $4.0 million or the year ended June 30, 2024. Losses associated with our investments in marketable and non-marketable equity securities were partially offset by We also recognized a gain attributable to equity method investments for the year ended June 30, 2025 2026 of $3.6 $7 million, compared to a loss gain of $1.8 $4 million for the year ended June 30, 2024. 2025. Interest income, net, and gains attributable to equity method investments were partially offset by losses associated with our investments in marketable and non-marketable equity securities of $15 million for the year ended June 30, 2026 compared to a loss of $10 million or the year ended June 30, 2025.

Source: Item 7, 10-K 0000943819-26-000047 vs Item 7, 10-K 0000943819-25-000035

Every change, by type

Sentences and paragraphs of RMD's Risk Factors and MD&A, 10-K 2026-08-13 against 10-K 2025-08-08. 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
•Failure to identify, execute, and integrate acquired businesses into our operations successfully, or challenges related to the Company's strategic initiatives, including divestitures.

Read it in 10-K 2026-08-13 at sec.gov ↗

AddedRisk Factors
•Our use of artificial intelligence in certain products, software solutions and business operations may expose us to operational, regulatory and reputational risks that could adversely affect our business, financial condition and results of operations.

Read it in 10-K 2026-08-13 at sec.gov ↗

AddedRisk Factors
We are subject to new areas of direct healthcare oversight by federal government agencies due to our acquisitions of VirtuOx and Noctrix. In 2025, we acquired VirtuOx, a software-enabled independent diagnostic testing facility, or IDTF, and provider of technology solutions to facilitate in-home and remote testing services for sleep, respiratory, cardiac, and other health conditions across the U.S. Additionally, in June 2026, we acquired Noctrix, a DME supplier and manufacturer of a neurostimulation FDA-cleared device to treat restless legs syndrome. As a Medicare-enrolled IDTF, VirtuOx, and as a

Read it in 10-K 2026-08-13 at sec.gov ↗

AddedRisk Factors
Failure to identify, execute, and integrate acquired businesses into our operations successfully, or challenges related to the Company's strategic initiatives, including divestitures. As part of our strategy to develop and identify new solutions and technologies and optimize our portfolio of products, we have completed several acquisitions and investments and may make additional acquisitions, investments, or divestitures in the future. Our integration of the operations of acquired businesses, or a divestiture of part of our existing businesses, including the separation of our MatrixCare business, requires significant efforts, including the coordination of information technologies, research and development, sales and marketing, operations, manufacturing, and finance. These efforts result in additional expenses, and our management may have attention diverted while trying to integrate acquisitions. In addition, the cumulative effect of simultaneously executing multiple transactions may increase operational complexity and heighten execution and timing risks. Our ability to realize the anticipated benefits of acquisitions depends not only on the successful integration of acquired businesses, but also on our ability to identify appropriate acquisition targets, evaluate their strategic fit and long‑term value, accurately assess risks and liabilities, and negotiate and complete transactions on acceptable terms. Our acquisitions may involve the undertaking of additional risk areas and the investment of additional resources and personnel to manage that risk. In addition, we cannot be certain that the businesses we acquire will become profitable or remain profitable. We also could experience negative effects on our business, results of operations, financial condition, and cash flows from acquisition-related charges, and amortization of intangible assets. Moreover, we have recorded intangible assets, including goodwill, in connection with our acquisitions. We evaluate goodwill for impairment annually and other acquired intangible assets whenever events or changes in circumstances indicate that their carrying values may not be recoverable. Our impairment assessments require significant judgments and assumptions, including those related to macroeconomic conditions, industry and market trends, projected revenues and cash flows, and discount rates. If actual results differ from these assumptions or market conditions change, we may be required to record material impairment charges that could adversely affect our results of operations. These effects, combined with transaction costs, retention or separation‑related expenses, and potential delays in realizing anticipated synergies or strategic benefits, may place pressure on earnings or cash flows.

Read it in 10-K 2026-08-13 at sec.gov ↗

AddedRisk Factors
In addition, expected strategic benefits from any planned or completed divestiture, including the separation of our MatrixCare business, may not be realized or may take longer to realize than expected, and there can be no assurance that disputes will not arise under transition service, or other agreements that have or may be executed as part of a divestiture. Challenges associated with executing these transactions may materially adversely affect our business, results of operations, financial condition, and cash flows.

Read it in 10-K 2026-08-13 at sec.gov ↗

AddedRisk Factors
Further, if we fail to innovate or adequately invest in new technologies, we could lose our competitive position in the markets that we serve. To the extent that we fail to introduce new and innovative products, or such products are not accepted or suffer significant delays in development, our financial results may suffer. An inability, for technological or other reasons, to successfully develop and introduce new products on a timely basis could reduce our growth rate or otherwise have an adverse effect on our business.

Read it in 10-K 2026-08-13 at sec.gov ↗

AddedRisk Factors
On June 9, 2025, CMS finalized a National Coverage Determination (NCD) entitled “Noninvasive Positive Pressure Ventilation (NIPPV) in the Home for the Treatment of Chronic Respiratory Failure (CRF) Consequent to Chronic Obstructive Pulmonary Disease (COPD).” The NCD establishes a uniform national coverage criteria for Respiratory Assist Devices (RADs) with bi-level capacity, with or without a backup rate feature, and for the first time, Home Mechanical Ventilators (HMVs) for patients with chronic respiratory failure (CRF) consequent to COPD. CMS subsequently issued implementation guidance on August 21, 2025 instructing Medicare contractors to process claims under the NCD effective June 9, 2025. Although the NCD establishes national coverage criteria that may reduce reimbursement uncertainty and replace previously applicable local coverage determination (LCD) policies for this indication, it also imposes specific clinical qualification, documentation, and ongoing patient monitoring requirements. The extent to which these national coverage criteria and associated operational requirements will affect providers, suppliers, utilization of these products, or reimbursement by other third-party payors remains uncertain.

Read it in 10-K 2026-08-13 at sec.gov ↗

AddedRisk Factors
On July 4, 2025, President Trump signed the budget reconciliation bill (entitled “One Big Beautiful Bill Act”, referred to herein as the “Bill”) to meet spending targets aimed at funding the Trump Administration’s domestic priorities that includes significant changes to the Medicaid program. Among other things, the Bill includes changes to Medicaid eligibility and enrollment requirements, provider taxes, and state-directed payment policies that are intended to reduce federal Medicaid spending over time. According to the Congressional Budget Office (CBO), the Bill is projected to reduce

Read it in 10-K 2026-08-13 at sec.gov ↗

AddedRisk Factors
federal spending on Medicaid and Marketplace coverage by approximately $1.1 trillion over the 2025-2034 period, increase the federal deficit by approximately $3.4 trillion on a conventional scoring basis over the same period, and result in approximately 10 million additional uninsured individuals by 2034. CBO has also estimated that, after accounting for macroeconomic effects, the Bill could increase federal deficits by approximately $4. trillion over the budget window.

Read it in 10-K 2026-08-13 at sec.gov ↗

AddedRisk Factors
In February 2026, the CBO projected that federal health programs will cost over $26 trillion through 2036, projected to grow in size from less than $2 trillion today to over $3 trillion by 2036. Medicare spending is projected to nearly double over the next decade, while the cost of Medicaid and the Children’s Health Insurance Program (CHIP) will grow a projected 36% and ACA subsidies by 33%. Finally, Medicare’s Hospital Insurance Trust Fund is projected to become insolvent in 2040, highlighting the continuing fiscal pressures facing the Medicare program. Future legislative and other governmental actions to curb this projected spending could include stricter eligibility requirements and more restrictive Medicaid programs at the state level, leaving fewer individuals eligible for coverage, which could have an adverse impact on the number of individuals who seek to use our products and services.

Read it in 10-K 2026-08-13 at sec.gov ↗

AddedRisk Factors
With respect to our recent acquisition of Noctrix, we may realize reductions in both reimbursement rates and coverage for the restless legs syndrome device, due to Noctrix not yet having a national or local coverage determination. To the extent that any Medicare administrative contractor decides that the restless legs syndrome product is not medically necessary or has not met applicable coverage criteria, claims for products could be denied and overpayments could be assessed. Further, any future coverage determination could implement more restrictive coverage requirements, including potential noncoverage entirely. As a new product, we cannot predict how the Medicare Program and its contractors will view the Noctrix device and its efficacy in the treatment of restless legs syndrome. If more restrictive coverage is implemented, our Noctrix revenues could be reduced.

Read it in 10-K 2026-08-13 at sec.gov ↗

AddedRisk Factors
participation in Federal healthcare programs. Violations of the Federal Anti-Kickback Statute can also result in significant criminal penalties and imprisonment;

Read it in 10-K 2026-08-13 at sec.gov ↗

RemovedRisk Factors
revenue, lower prices for our products, or reduced reimbursement rates by third-party payors, while increasing the cost of operating our business.

Read it in 10-K 2025-08-08 at sec.gov ↗

RemovedRisk Factors
We may not be able to realize the anticipated benefits from acquisitions, which could adversely affect our operating results. Part of our growth strategy includes acquiring businesses consistent with our commitment to innovation in developing products for the diagnosis and treatment of sleep apnea and related breathing health as well as our Residential Care Software business. The success of our acquisitions depends, in part, on our ability to successfully identify, acquire and integrate the business and operations of the target companies. Additionally, our management may have attention diverted while trying to integrate acquisitions. If we are not able to successfully integrate the operations of acquisitions, we may not realize the anticipated benefits fully or at all, or may take longer to realize than expected. Acquisitions involve numerous risks and could create unforeseen operating difficulties and expenditures. As noted above, our acquisition of VirtuOx involves the undertaking of additional risk areas and the investment of additional resources and personnel to manage that risk. It is possible that our return on investment is not realized given our investment of such additional

Read it in 10-K 2025-08-08 at sec.gov ↗

RemovedRisk Factors
Moreover, we have recorded intangible assets, including goodwill, in connection with our acquisitions. At least on an annual basis, we must evaluate whether facts and circumstances demonstrate any impairment of the value of acquired intangible assets. The qualitative and quantitative analysis used to test goodwill is dependent upon various considerations and assumptions, including macroeconomic conditions, industry and market characteristics, projections of acquired companies’ future revenue, discount rates, and expectations of future cash flows. While we have made such assumptions in good faith and believe them to be reasonable, the assumptions may turn out to be materially inaccurate, including for reasons beyond our control. Changes in such assumptions may cause a change in circumstances demonstrating that the carrying value of intangible assets may be impaired. Consequently, we may be required to record a significant charge to earnings in the financial statements during the period in which any impairment of intangible assets is determined.

Read it in 10-K 2025-08-08 at sec.gov ↗

RemovedRisk Factors
On June 9, 2025, CMS released long-awaited Medicare guidance on coverage and reimbursement for respiratory assist devices with bi-level capacity and mechanical ventilators when used in the home for the treatment of chronic respiratory failure consequent to COPD; a new CMS national coverage determination is expected in September 2025. Although national reimbursement criteria may ease existing reimbursement uncertainty over these items for this indication, it is unclear how national coverage criteria and associated documentation requirements will impact providers and suppliers who invoice Medicare directly; third-party payors may also follow suit in implementing similar policies.

Read it in 10-K 2025-08-08 at sec.gov ↗

RemovedRisk Factors
On July 4, 2025, President Trump signed the budget reconciliation bill (entitled “One Big Beautiful Bill Act”, referred to herein as the “Bill”) to meet spending targets aimed at funding the Trump Administration’s domestic priorities that includes significant changes to the Medicaid program. A July 21, 2025 estimate by the Congressional Budget Office (CBO) indicates that the bill will reduce the federal deficit by $366 billion over the next 10 years, due to decreased direct spending. Earlier June 2025 CBO preliminary estimates also showed that the Medicaid provisions of the bill would reduce Medicaid spending by approximately $1 trillion and would increase the number of people without health insurance by at least 11.8 million by 2034. Some key proposed changes to the Medicaid Program include, but are not limited to: work requirements; cost sharing of up to $35 per service on expansion adults who exceed the official poverty threshold; stricter eligibility requirements for non-U.S. citizens; requirements for states to conduct eligibility redeterminations at least every 6 months for Medicaid expansion adults; and prohibitions on states from establishing any new provider taxes or from increasing the rates of existing taxes, among other changes. Decreased federal funding and stricter eligibility requirements may result in more restrictive Medicaid programs at the state level and less individuals eligible for coverage, which could have an adverse impact on the number of individuals who seek to use our products and services.

Read it in 10-K 2025-08-08 at sec.gov ↗

RemovedRisk Factors
reimbursement. Decreases in third-party reimbursement for our products or a decision by a third-party payor to not cover our products as a result of a third-party study could have a material adverse effect on our sales, results of operations and financial condition.

Read it in 10-K 2025-08-08 at sec.gov ↗

RemovedRisk Factors
In December 2019, we entered into a settlement agreement with the U.S. Department of Justice and the U.S. Attorneys’ Offices for the District Court of South Carolina, the Southern District of California, the Northern District of Iowa and the Eastern District of New York. The agreement resolved five lawsuits originally brought by whistleblowers under the qui tam provisions of the False Claims Act and allegations that we: (a) provided DME companies with free telephone call center services and other free patient outreach services that enabled these companies to order resupplies for their patients with sleep apnea, (b) provided sleep labs with free and below-cost positive airway pressure masks and diagnostic machines, as well as free installation of these machines, (c) arranged for, and fully guaranteed the payments due on, interest-free loans that DME supplies acquired from third-party financial institutions for the purchase of our equipment, and (d) provided non-sleep specialist physicians free home sleep testing devices referred to as “ApneaLink.” We agreed with the government to civilly resolve these matters for a payment of $39.5 million ($37.5 million to the federal government and $2 million to the various states) and we incurred additional fees and administrative costs that typically accompany such a resolution amounting to $1.1 million. The specific allegations and the resolution of those allegations are contained in the Company’s settlement agreement with the adverse parties. The total final costs relating to these matters were $40.6 million.

Read it in 10-K 2025-08-08 at sec.gov ↗

RemovedRisk Factors
Contemporaneous with the civil settlement, we also entered into a five-year Corporate Integrity Agreement, or CIA, with the Department of Health and Human Services Office of Inspector General, or OIG. The CIA required, among other things, that we implement additional controls around our product pricing and sales and that we conduct internal and external monitoring of our arrangements with referrals sources. Our failure to comply with our obligations under the CIA could result in monetary penalties and our exclusion from participating in federal healthcare programs. The costs associated with compliance with the CIA, or any liability or consequences associated with its breach, could have an adverse effect on our operations, liquidity and financial condition. Most of the obligations of the CIA expired on December 18, 2024. Absent an inquiry for additional materials from the OIG, we expect to close out the CIA shortly after the end of fiscal year 2025.

Read it in 10-K 2025-08-08 at sec.gov ↗

RemovedRisk Factors
business associate agreements often have shorter notification timeframes which we are required to abide by contractually. We could also face contractual liability if we fail to meet our obligations under our business associate agreements.

Read it in 10-K 2025-08-08 at sec.gov ↗

RemovedRisk Factors
disagrees with us and requires us to submit new Section 510(k) notifications for modifications to our existing products, we may be required to stop marketing the products while the FDA reviews the Section 510(k) notification.

Read it in 10-K 2025-08-08 at sec.gov ↗

RewordedRisk Factors
Additionally, while several countries, including the U.S. and other members of the Organization for Economic Co-operation and Development, or OECD, have reached agreement on a global minimum income tax initiative, or Pillar Two, on June 28, 2025, January 1, 2026, the G7 issued a joint statement in OECD released the Side-by-Side, or SbS, Package, which its members agreed that exempts U.S.-headquartered multinational enterprises from Pillar Two will operate alongside the U.S. system of tax and proposed that U.S.-parented multinational groups would not be subject to the Two’s income inclusion rules and undertaxed profits profit rules of Pillar Two. for tax years beginning on or after January 1, 2026.

Read it in 10-K 2026-08-13 at sec.gov ↗

RewordedRisk Factors
In addition, the calculation of our tax liabilities involves dealing with uncertainties in the application of complex tax laws. laws, including current and evolving government policies that encourage the establishment or relocation of certain activities, such as manufacturing, research and development, information technologies, and other business operations in their jurisdictions.

Read it in 10-K 2026-08-13 at sec.gov ↗

RewordedRisk Factors
Any interruptions or delays in our service, whether caused by our products, or as a result of third-party error, our own error, natural disasters or security breaches, whether accidental or willful, could harm our relationships with customers and cause our revenue to decrease and/or our expenses to increase.

Read it in 10-K 2026-08-13 at sec.gov ↗

RewordedRisk Factors
We have assessed the impact of the laws in effect as of June 30, 2025 2026, and anticipate that the Pillar Two minimum tax had a material impact on our income tax expense and cash flows during the fiscal year ended June 30, 2026 and may continue to impact our effective tax rate in fiscal year 2026. 2027.

Read it in 10-K 2026-08-13 at sec.gov ↗

RewordedRisk Factors
The impacts of climate change may include physical risks (such as frequency and severity of extreme weather conditions), social and human effects (such as population dislocations or harm to health and well-being), compliance costs and transition risks (including due to regulatory changes), shifts in market trends (including customer preference for sustainably produced or reusable products) and other adverse effects.

Read it in 10-K 2026-08-13 at sec.gov ↗

RewordedRisk Factors
Many In addition, many prospective customers have invested substantial personnel and financial resources to create, implement and integrate their current existing business management software into their operations and, therefore, and may therefore be reluctant or unwilling to change from their current in-house solution or provider switch to one of our platforms or products.

Read it in 10-K 2026-08-13 at sec.gov ↗

RewordedRisk Factors
Our business depends on our ability to market effectively to educate and engage dealers of home healthcare products, sleep clinics, clinics and physicians. physicians, health care providers, and patients regarding the benefits of our products, software solutions and services.

Read it in 10-K 2026-08-13 at sec.gov ↗

RewordedRisk Factors
Deterioration in the global economic environment may cause decreased demand for our products and services which could result in lower product sales, services revenue, lower prices for our products, or reduced reimbursement rates by third-party payors, while increasing the cost of operating our business.

Read it in 10-K 2026-08-13 at sec.gov ↗

RewordedRisk Factors
Sales in combined Europe, Asia and other Rest of World regions accounted for approximately 36% 37% and 36% of our net revenues in the years ended June 30, 2026 and June 30, 2025, respectively.

Read it in 10-K 2026-08-13 at sec.gov ↗

RewordedRisk Factors
Accordingly, it is unclear the extent to which any proposals, if adopted, could impose additional regulatory requirements on us that could delay our ability to obtain new 510(k) clearances, increase the costs of compliance, or restrict our ability to maintain our current clearances, or otherwise create competition that may negatively affect our business.

Read it in 10-K 2026-08-13 at sec.gov ↗

RewordedRisk Factors
The Many of the remaining OECD countries are in the process of implementing the SbS package in local legislation to align with the OECD. likely to consider changes to existing and proposed tax laws to align with the recommendations and guidelines proposed by G7.

Read it in 10-K 2026-08-13 at sec.gov ↗

RewordedRisk Factors
Tax laws, regulations, and enforcement practices are evolving, are aggressively pursued This may result in some jurisdictions, and may cause expense as well as management distraction, which may result in a material adverse effect on our results of operations, cash flows and financial position.

Read it in 10-K 2026-08-13 at sec.gov ↗

Quiet changesRisk Factors
The UK GDPR mirrors the fines under the EU GDPR, i.e., fines up to the greater of £17.5 approximately £18 million or 4% of global turnover.

Read it in 10-K 2026-08-13 at sec.gov ↗

AddedMD&A
We are a global leader in digital health and cloud-connected medical devices. We design innovative technology with the intention to empower people to live happier, healthier lives. Our artificial intelligence, or AI, powered digital health solutions, cloud-connected devices and intelligent software are designed to make home healthcare more personalized, accessible and effective. By enabling better care, our products seek to improve quality of life, reduce the impact of chronic disease, and lower costs for consumers and healthcare systems.

Read it in 10-K 2026-08-13 at sec.gov ↗

AddedMD&A
In June 2026, we acquired Noctrix Health, LLC, or Noctrix, a company with an FDA De Novo classified medical device that treats restless legs syndrome. The acquisition expands our clinical sleep health portfolio into an adjacent area of unmet need. Noctrix will operate as a wholly owned subsidiary of Resmed.

Read it in 10-K 2026-08-13 at sec.gov ↗

AddedMD&A
On June 30, 2026, we entered into a definitive agreement to sell our MatrixCare business for $490 million in an all-cash transaction, subject to certain closing adjustments. The transaction includes MatrixCare and related software offerings historically sold under the MatrixCare brand, including Healthcare First, Citus, and home health and hospice solutions, collectively defined as the "MatrixCare business”. The transaction is expected to close in the first quarter of fiscal year 2027. During fiscal year 2026, the MatrixCare business represented approximately $220 million of revenue and approximately $28 million of operating profit, which included approximately $28 million of amortization from acquired intangibles. As of June 30, 2026, we determined that the MatrixCare business meets the criteria to be classified as held for sale. The results of operations of the MatrixCare business are included in continuing operations for all periods presented, as the disposition does not represent a strategic shift that will have a major effect on our operations or financial results and therefore does not meet the criteria to be classified as discontinued operations. Additional information regarding the sale of the MatrixCare business and the acquisition of Noctrix is included in Note 18 – Business Combinations and Divestitures of the Notes to Consolidated Financial Statements (Part II, Item 8).

Read it in 10-K 2026-08-13 at sec.gov ↗

AddedMD&A
(B) Historically we have presented our geographical split of revenue as “U.S., Canada, and Latin America” and “Combined Europe, Asia, and other markets”. Effective this quarter, this presentation has been renamed to Americas (formerly U.S., Canada, and Latin America) and Rest of World (formerly Combined Europe, Asia, and other markets). The methodology for attributing revenue to these geographies remains unchanged. Revenue from prior periods is consistent and comparable to previous reporting.

Read it in 10-K 2026-08-13 at sec.gov ↗

AddedMD&A
When a portion of a reporting unit is classified as held for sale, goodwill is allocated to the disposal group based on the relative fair values of the disposal group and the portion of the reporting unit that will be retained. The goodwill allocated to the disposal group is included in the carrying amount of the disposal group for purposes of measuring any gain or loss on sale and is no longer subject to separate annual or interim impairment testing. See Note 18 – Business Combinations and Divestitures of the Notes to Consolidated Financial Statements (Part II, Item 8) for further information.

Read it in 10-K 2026-08-13 at sec.gov ↗

RemovedMD&A
We are a global leader in the development, manufacturing, distribution and marketing of medical devices and cloud-based software applications that diagnose, treat and manage respiratory disorders, including sleep disordered breathing, or SDB, chronic obstructive pulmonary disease, neuromuscular disease and other chronic diseases. SDB includes obstructive sleep apnea and other respiratory disorders that occur during sleep. Our products and solutions are designed to improve patient quality of life, reduce the impact of chronic disease and lower healthcare costs as global healthcare systems continue to drive a shift in care from hospitals to the home and lower cost settings. Our digital cloud-based health software applications, along with our devices, are designed to provide connected care to improve patient outcomes and efficiencies for our customers.

Read it in 10-K 2025-08-08 at sec.gov ↗

RemovedMD&A
Amortization of acquired intangible assets for the year ended June 30, 2025 was $45.3 million compared to $46.5 million for the year ended the year ended June 30, 2024. The decrease in amortization of acquired intangibles is due to certain acquired intangible assets reaching the end of their useful lives and becoming fully amortized, partially offset by increases from amortization of acquired intangibles associated with new acquisitions.

Read it in 10-K 2025-08-08 at sec.gov ↗

RemovedMD&A
When Sleep and Breathing Health or Residential Care Software contracts have multiple performance obligations, we generally use an observable price to determine the stand-alone selling price by reference to pricing and discounting practices for the specific product or service when sold separately to similar customers. Revenue is then allocated proportionately, based on the determined stand-alone selling price, to each performance obligation. An allocation is not

Read it in 10-K 2025-08-08 at sec.gov ↗

RemovedMD&A
required for many of our Sleep and Breathing Health contracts that have a single performance obligation, which is the shipment of our therapy-based equipment.

Read it in 10-K 2025-08-08 at sec.gov ↗

RewordedMD&A
Year Ended June 30, 2026 2025 2024 GAAP net income $ 1,523,293 $ 1,400,723 $ 1,020,951 Amortization of acquired intangibles - cost of sales 31,779 32,116 32,963 Amortization of acquired intangibles - operating expenses 45,466 45,273 46,521 Restructuring expenses 21,745 — 64,228 Masks with magnets field safety notification expenses — (1,512) 6,351 Astral field safety notification expenses 41,885 — 7,911 Acquisition-related Acquisition and portfolio review related expenses 11,486 2,031 483 Gain on previously held equity investment (4,353) — Tax benefit from business cessation — (21,430) — Income tax effect of interest income on tax refunds — (29,976) — Income tax effect on non-GAAP adjustments (39,453) (20,448) (40,114) Non-GAAP net income $ 1,631,848 $ 1,406,777 $ 1,139,294 Diluted shares outstanding 146,054 147,340 147,550 GAAP diluted earnings per share $ 10.43 $ 9.51 $ 6.92 Non-GAAP diluted earnings per share $ 11.17 $ 9.55 $ 7.72

Read it in 10-K 2026-08-13 at sec.gov ↗

RewordedMD&A
Year Ended June 30, 2026 2025 2024 GAAP net revenue $ 5,653,443 $ 5,146,327 GAAP income from operations $ 1,886,715 $ 1,685,363 $ 1,319,893 Amortization of acquired intangibles - cost of sales 31,779 32,116 32,963 Amortization of acquired intangibles - operating expenses 45,466 45,273 46,521 Restructuring expenses 21,745 — 64,228 Masks with magnets field safety notification expenses — (1,512) 6,351 Astral field safety notification expenses 41,885 — 7,911 Acquisition-related Acquisition and portfolio review related expenses 11,486 2,031 483 Non-GAAP income from operations $ 2,039,076 $ 1,763,271 $ 1,478,350 GAAP operating margin 33.4 % 32.7 % Non-GAAP operating margin 36.1 % 34.3 %

Read it in 10-K 2026-08-13 at sec.gov ↗

RewordedMD&A
We recorded interest income, net, of $4.1 $50 million for the year ended June 30, 2026 compared to interest income, net, of $4 million for the year ended June 30, 2025 compared to interest expense, net of $45.7 million for the year ended June 30, 2024 due to lower debt levels following the repayment of our revolving credit facility facility, gains recognized on cross-currency swaps associated with our fair value and net investment hedges, and interest earned on cash balances.

Read it in 10-K 2026-08-13 at sec.gov ↗

RewordedMD&A
The increase in gross margin was due primarily to procurement, manufacturing and logistics efficiencies, $14.3 million of combined partially offset by expenses associated with the a field safety notifications notification for masks with magnets and Astral devices recognized during in the year ended June 30, 2024, as well as a reduction in the amortization of acquired intangibles during the year ended June 30, 2025. 2026.

Read it in 10-K 2026-08-13 at sec.gov ↗

RewordedMD&A
The measure “non-GAAP net income” income from operations” is equal to GAAP net income from operations once adjusted for amortization of acquired intangibles, restructuring expenses, field safety notification expenses, and acquisition and portfolio review related expenses, and associated tax effects, in addition to tax benefits from business cessation, and the tax effect of interest and penalties on tax refunds. expenses.

Read it in 10-K 2026-08-13 at sec.gov ↗

RewordedMD&A
The decrease increase in our effective tax rate for the year ended June 30, 2025 2026 was primarily due to driven by the IRS implementation of the Pillar Two global minimum tax and certain non-recurring tax benefits recognized during the year ended June 30, 2025, including the refund of interest and penalties from the IRS and tax benefits realized from the cessation of certain business activities.

Read it in 10-K 2026-08-13 at sec.gov ↗

RewordedMD&A
Net revenue from masks and other for the year ended June 30, 2025 2026 increased to $1,839.7 $2,085 million from $1,657.2 $1,840 million for the year ended June 30, 2024, 2025, an increase of 11%, 13%, including an increase of 12% 13% in the U.S., Canada and Latin America Americas and an increase of 15% in Rest of World (a 9% in combined Europe, Asia and other markets (an 8% increase on a constant currency basis).

Read it in 10-K 2026-08-13 at sec.gov ↗

RewordedMD&A
Net revenue from devices for the year ended June 30, 2025 2026 increased to $2,665.2 $2,892 million from $2,444.0 $2,665 million for the year ended June 30, 2024, 2025, an increase of $221.2 $227 million or 9%, including an increase of 9% 7% in the U.S., Canada and Latin America Americas and an increase of 10% 11% in combined Europe, Asia and other markets Rest of World (a 9% 6% increase on a constant currency basis).

Read it in 10-K 2026-08-13 at sec.gov ↗

RewordedMD&A
Since the development of continuous positive airway pressure therapy, we have expanded our business by developing or acquiring a number of innovative products and solutions for a broader broad range of respiratory sleep and related breathing health disorders including technologies to be applied in medical and consumer products, life support and ventilation devices, diagnostic products, mask systems for use in the hospital and home, headgear and other accessories, and dental devices, and cloud-based software informatics solutions to manage patient outcomes and customer and provider business processes. devices.

Read it in 10-K 2026-08-13 at sec.gov ↗

RewordedMD&A
Net Excluding the impact of foreign currency movements, net revenue from our Residential Care Software business for the year ended June 30, 2025 was $641.4 million, 2026 increased by 4% compared to $584.1 million for the year ended June 30, 2024, an increase of $57.3 million or 10%. 2025.

Read it in 10-K 2026-08-13 at sec.gov ↗

RewordedMD&A
The $69.7 $345 million decrease increase in cash flow used in investing activities was primarily due to cash used for business acquisitions, including for the acquisition of Noctrix, increased purchases of property, plant and equipment, and lower net proceeds from maturity of foreign currency contracts during the year ended June 30, 2025 compared to net 2026.

Read it in 10-K 2026-08-13 at sec.gov ↗

RewordedMD&A
Losses associated with our investments in marketable and non-marketable equity securities were partially offset by We also recognized a gain attributable to equity method investments for the year ended June 30, 2025 2026 of $3.6 $7 million, compared to a loss gain of $1.8 $4 million for the year ended June 30, 2024. 2025.

Read it in 10-K 2026-08-13 at sec.gov ↗

Work on RMD in a spreadsheet: Excel workbook (a sheet per section, ten years by column, charts, links to the filings) · CSV. For a Google Sheet that stays up to date, paste =IMPORTDATA("https://tickdelta.com/company/RMD/export.csv") into a cell.