Aug 13, 2026
By Emily Martin
Medtronic is one of the world’s largest diversified medical-technology companies. Its fiscal 2026 results show a business with US$36.364 billion in net sales, a broad installed base across cardiovascular, neuroscience, surgical and diabetes care, and annual R&D spending approaching US$2.9 billion. In this article, Medtronic statistics refer primarily to the 52-week fiscal year ended 24 April 2026, not the calendar year.
The strongest top-line momentum came from Cardiovascular and Diabetes. The year also changed how investors should read the portfolio: following the March 2026 initial public offering of MiniMed, Medtronic stopped treating Diabetes as a reportable segment in its fourth quarter disclosure, although the business remained consolidated during FY2026.
| Company metric | Verified information |
| Legal name | Medtronic plc |
| Founded | 1949 |
| Founders | Earl Bakken and Palmer Hermundslie |
| Registered office / domicile | Galway, Ireland |
| Operational headquarters | Minneapolis area, Minnesota, United States |
| Chief executive officer | Geoff Martha (as of 12 August 2026) |
| Industry | Healthcare technology and medical devices |
| Company type | Irish public limited company |
| Stock exchange | New York Stock Exchange |
| Ticker | MDT |
| Latest employee count | More than 95,000 full-time employees (FY2026 filing) |
| Geographic presence | Global sales and operations; FY2026 filing reports U.S. and international revenue |
| Principal reportable segments | Cardiovascular, Neuroscience and Medical Surgical; Diabetes aggregated in Other after MiniMed IPO |
| Official website | https://www.medtronic.com/ |
Medtronic designs, manufactures and sells implantable devices, capital equipment, instruments, consumables, software and monitoring systems. Hospitals and clinicians use its products in cardiology, cardiac surgery, vascular intervention, neurosurgery, spine surgery, pain management, general surgery, intensive care and diabetes management. Patients also interact directly with long-duration technologies such as pacemakers, neurostimulators, insulin pumps and connected monitoring systems.
The customer base includes hospitals, ambulatory surgery centers, physician practices, distributors, purchasing organizations and public health systems. Revenue comes from a mix of implanted devices, disposable instruments and sensors, service arrangements, software and repeat consumables. This combination creates both procedure-sensitive sales and recurring demand tied to installed platforms.
At FY2026 year-end, the reporting structure comprised Cardiovascular, Neuroscience and Medical Surgical. Diabetes remained an operating business but was aggregated with “Other” after Medtronic sold 10% of MiniMed through an IPO and stated its intention to divest the remaining interest. That distinction matters when comparing segment disclosures across years.
| Year | Verified milestone |
| 1949 | Earl Bakken and Palmer Hermundslie established a medical-equipment repair business in Minneapolis. |
| 1950s | Bakken developed a wearable, battery-powered external pacemaker after a hospital power failure highlighted the need for portable pacing. |
| 1960s–1980s | Medtronic expanded implantable pacing and entered additional cardiovascular, neurological and surgical fields. |
| 1990s–2000s | The company broadened through product development and acquisitions in spine, diabetes, vascular and neuromodulation technologies. |
| 2015 | Medtronic completed its acquisition of Covidien; the combined parent became Medtronic plc, domiciled in Ireland. |
| 2020–2022 | Pandemic disruption affected elective procedures; Medtronic continued product investment and initiated organizational simplification. |
| 2023 | Medtronic and DaVita formed Mozarc Medical from the Renal Care Solutions business. |
| 2024 | The company announced an exit from the ventilator product line while retaining acute-care monitoring businesses. |
| 2025 | Medtronic announced plans to separate Diabetes as MiniMed and received FDA clearance for Hugo robotic-assisted surgery in urology. |
| 2026 | MiniMed completed an IPO of a 10% stake; Medtronic completed Scientia Vascular and SPR Therapeutics acquisitions and issued FY2027 guidance. |
| Fiscal year | Net sales (US$ bn) | YoY growth |
| FY2022 | 31.686 | — |
| FY2023 | 31.227 | -1.4% (calculated) |
| FY2024 | 32.364 | 3.6% (calculated) |
| FY2025 | 33.537 | 3.6% (calculated) |
| FY2026 | 36.364 | 8.4% (calculated) |
Net sales declined 1.4% in FY2023, then resumed growth. FY2024 and FY2025 increased 3.6% each on a calculated reported basis. FY2026 accelerated to 8.4% reported, while Medtronic’s organic measure was 5.8%. Reported growth benefited from foreign exchange and a US$39 million Italian payback adjustment; organic growth removes currency and specified inorganic or accounting effects.
Cardiac ablation, leadless pacing, structural heart products, renal denervation, neuromodulation, monitoring, surgical technologies and diabetes systems supported growth. The filing also identifies constraints including tariffs, foreign exchange volatility, product mix, supply availability, reimbursement and procedure trends.

FY2026 produced the strongest reported annual growth in the five-year series.
| Metric | FY2024 | FY2025 | FY2026 |
| Operating profit (US$ bn) | 5.144 | 5.955 | 6.467 |
| Operating margin (calculated) | 15.9% | 17.8% | 17.8% |
| Net income attributable (US$ bn) | 3.676 | 4.662 | 4.801 |
| Diluted EPS | US$2.76 | US$3.61 | US$3.73 |
| Adjusted diluted EPS | US$5.20 | US$5.49 | US$5.53 |
| Operating cash flow (US$ bn) | 6.787 | 7.044 | 7.330 |
| Free cash flow (US$ bn) | Not shown here | 5.185 | 5.426 |
| Dividend per share | US$2.76 | US$2.80 | US$2.84 |
Profit growth was slower than revenue growth at the bottom line. GAAP net income rose 3.0% and diluted EPS rose 3.3% in FY2026. The operating margin was approximately 17.8% in both FY2025 and FY2026 when calculated from GAAP operating profit and sales. Adjusted operating margin fell 130 basis points, reflecting investment, tariffs and other operating factors described by management.
| Business | FY2026 US$bn | FY2025 US$bn | YoY | Share |
| Cardiovascular | 13.976 | 12.481 | 12.0% calc. | 38.4% calc. |
| Neuroscience | 10.287 | 9.846 | 4.5% calc. | 28.3% calc. |
| Medical Surgical | 8.815 | 8.407 | 4.9% calc. | 24.2% calc. |
| Diabetes | 3.112 | 2.755 | 13.0% calc. | 8.6% calc. |
Cardiovascular was the largest business. Within it, Cardiac Rhythm & Heart Failure generated US$7.504 billion, Structural Heart & Aortic US$3.817 billion, and Coronary & Peripheral Vascular US$2.656 billion. Neuroscience included Cranial & Spinal Technologies (US$5.222 billion), Specialty Therapies (US$2.997 billion) and Neuromodulation (US$2.068 billion).
Medical Surgical comprised Surgical & Endoscopy (US$6.764 billion) and Acute Care & Monitoring (US$2.051 billion). Diabetes sales reached US$3.112 billion, but the company no longer presented Diabetes as a reportable segment at year-end because of the MiniMed separation pathway.

Cardiovascular contributed about 38% of consolidated FY2026 net sales.
| Geography | FY2026 net sales | FY2025 net sales | YoY change | FY2026 share |
| United States | US$18.103bn | US$17.171bn | 5.4% calculated | 49.8% calculated |
| International | US$18.261bn | US$16.365bn | 11.6% calculated | 50.2% calculated |
Medtronic’s audited FY2026 filing uses U.S. and international as the directly comparable consolidated geography categories. It does not provide a full audited split between developed markets outside the U.S. and emerging markets in the segment table; therefore, no artificial regional estimates are added here. International growth outpaced U.S. growth, helped partly by currency translation.

International revenue narrowly exceeded U.S. revenue.
| Fiscal year | Full-time employees | Comparable note |
| FY2022 | About 95,000 | Annual-report count |
| FY2023 | More than 95,000 | Annual-report disclosure |
| FY2024 | More than 95,000 | Annual-report disclosure |
| FY2025 | More than 95,000 | Annual-report disclosure |
| FY2026 | More than 95,000 | 43% in U.S. or Puerto Rico |
The filing does not publish a precise FY2026 headcount or a full workforce split by manufacturing, research and commercial function. It reports that 43% of full-time employees were in the U.S. or Puerto Rico. Based on the “more than 95,000” disclosure, that percentage implies at least about 40,850 people in those locations, but the company does not provide an exact number.
Medtronic reported 100% U.S. pay equity for gender and ethnically diverse employees and 99% global gender pay equity for its most recently reported period. These are company-reported pay-equity measures, not workforce representation percentages. Restructuring charges totaled US$249 million in FY2026, but the 10-K does not equate that amount to a specified number of job reductions.
| Fiscal year | R&D expense | YoY | R&D / sales |
| FY2022 | US$2.493bn | — | 7.9% calc. |
| FY2023 | US$2.696bn | 8.1% calc. | 8.6% calc. |
| FY2024 | US$2.735bn | 1.4% calc. | 8.5% calc. |
| FY2025 | US$2.732bn | -0.1% calc. | 8.1% calc. |
| FY2026 | US$2.873bn | 5.2% calc. | 7.9% calc. |
R&D spending rose to a five-year high of US$2.873 billion in FY2026, up 5.2% from FY2025 on a calculated basis. The portfolio spans pulsed-field ablation, pacing and defibrillation, transcatheter heart valves, renal denervation, spine navigation, deep-brain and spinal-cord stimulation, diabetes automation, surgical robotics, artificial intelligence and connected-care software.
Medtronic’s investor site reports 180-plus active clinical trials in FY2026. The company also uses funded R&D arrangements; these should not be confused with GAAP R&D expense. For example, a US$157 million charge tied to a funded-development royalty obligation was recorded in other operating expense in FY2026.

R&D expense increased by roughly US$380 million over five years.
Cardiac rhythm. Pacemakers, leadless pacing systems, implantable cardioverter-defibrillators, cardiac-resynchronization devices, insertable monitors, leads and remote-care systems.
Cardiovascular intervention. Transcatheter and surgical valves, aortic stent grafts, coronary and peripheral devices, cardiac ablation systems and the Symplicity renal-denervation platform.
Diabetes. MiniMed insulin pumps, continuous glucose-monitoring sensors, infusion sets and automated insulin-delivery software.
Surgery and monitoring. LigaSure energy devices, stapling and suturing products, endoscopy tools, Nellcor oximetry, Microstream capnography, airway products and advanced monitoring sensors.
Neuroscience. Spine and cranial implants, imaging and navigation, deep-brain stimulation, spinal-cord stimulation and peripheral nerve stimulation.
Robotics and digital. The Hugo robotic-assisted surgery system, Stealth navigation, Touch Surgery Enterprise video analytics and connected device-management software.
Product breadth reduces dependence on any single therapy, but it also raises regulatory, manufacturing and quality-system complexity. Utilization varies with procedure volumes, clinical evidence, physician training, hospital capital budgets and reimbursement.
Medtronic’s FY2026 Form 10-K states that patents, trademarks, trade secrets and know-how are important, but it does not publish a reconciled count of active patents, granted patents, applications or patent families. Accordingly, this article does not present a headline patent total. Public patent databases can change as applications publish, rights lapse and ownership records update.
A granted patent is an issued right in one jurisdiction; an active patent is an issued patent still in force; an application is pending and may never issue; and a patent family groups related filings that claim common priority. Adding these categories together would double-count inventions and misstate portfolio size. Innovation evidence is therefore discussed through R&D expense, clinical trials, regulatory decisions and product launches.
| Date | Transaction / partner | Purpose and segment | Value / status |
| 26 Jan 2015 | Covidien acquisition completed | Global scale in surgical, monitoring and vascular technologies | Approx. US$49.9bn equity value; completed |
| 1 Apr 2023 | Mozarc Medical with DaVita | Independent kidney-care device company | Medtronic retained 50%; operating partnership |
| May 2025 | MiniMed separation announced | Create an independent diabetes company | IPO of 10% completed 9 Mar 2026; remaining divestiture planned |
| 3 Mar 2026 | CathWorks acquisition completed | AI-enabled FFRangio in coronary care | Up to US$585m total consideration under prior agreement |
| 10 Mar / 12 Jun 2026 | Scientia Vascular announced / completed | Neurovascular guidewires and catheters; Neuroscience | US$550m plus potential undisclosed earn-outs |
| May / 16 Jul 2026 | SPR Therapeutics announced / completed | Temporary peripheral nerve stimulation; Neuromodulation | US$650m upfront plus up to US$40m milestones |
| 2026 | Merit Medical distribution agreement | ViaVerte sacroiliac fusion system; Neuromodulation | Terms not disclosed |
| 2026 | Pulnovo Medical investment | Pulmonary-hypertension technology; Cardiovascular | Investment terms not disclosed |
| Date | Milestone | Regulatory meaning / business |
| 18 Apr 2025 | Simplera Sync sensor approved for MiniMed 780G | FDA approval; Diabetes continuous glucose monitoring integration |
| 3 Dec 2025 | Hugo RAS cleared for urologic procedures | FDA 510(k) clearance; Medical Surgical robotics |
| 23 Mar 2026 | OmniaSecure defibrillation lead approved | FDA premarket approval for a lead designed for conduction-system pacing; Cardiovascular |
| 27 Mar 2026 | Stealth AXiS cleared for cranial and ENT | FDA 510(k) clearance; Neuroscience navigation |
| 28 Apr 2026 | Stealth AXiS received CE Mark for spine and cranial indications | EU conformity certification enabling commercialization under applicable rules |
| 3 Jun 2026 | Hugo submissions disclosed for general surgery and gynecology | FDA review filing; not an approval or clearance |
| FY2026 Q4 | ProGrip Advanced cleared | FDA clearance; Medical Surgical product development |
“Approval,” “clearance,” “CE Mark,” “submission” and “launch” are not interchangeable. Approval generally reflects an FDA premarket approval pathway for higher-risk devices or supplemental indications; 510(k) clearance establishes substantial equivalence; CE Mark indicates conformity with European requirements; a submission remains under review; and a commercial launch describes market availability.
| Company | Latest annual revenue | Main areas | Employees | Period / scope |
| Medtronic | US$36.364bn | Cardiovascular, neuroscience, surgery, diabetes | >95,000 | FY ended 24 Apr 2026; total company |
| Abbott | US$44.3bn | Devices, diagnostics, nutrition, medicines | ≈114,000 | Year ended 31 Dec 2025; total company |
| Boston Scientific | US$20.074bn | Cardiovascular, endoscopy, urology, neuromodulation | ≈48,000 | Year ended 31 Dec 2025; total company |
| Stryker | ≈US$25.1bn | Orthopaedics, surgical, neurotechnology | ≈57,000 | Year ended 31 Dec 2025; total company |
| Johnson & Johnson | Segment disclosure | Surgery, orthopaedics, cardiovascular | Not separately reported | 2025 MedTech segment; not total J&J |
| Edwards Lifesciences | ≈US$6.0bn | Structural heart and critical care | ≈20,000 | Year ended 31 Dec 2025; total company |
| Becton Dickinson | US$21.8bn | Medication delivery, diagnostics, interventional | ≈75,000 | FY ended 30 Sep 2025; total company |
| Siemens Healthineers | ≈€23.4bn | Imaging, diagnostics, cancer care | ≈74,000 | FY ended 30 Sep 2025; total company |
| Philips | ≈€18.0bn | Imaging, monitoring, connected care | ≈64,000 | Year ended 31 Dec 2025; continuing operations |
This comparison is directional. Abbott and Philips include businesses beyond implanted devices; Johnson & Johnson does not publish a MedTech-only employee count; Siemens Healthineers reports in euros; and fiscal year-ends differ. Revenue scale alone does not measure market share in a specific therapy.
Medtronic’s competitive position rests on broad clinical coverage, an international commercial network, physician relationships, manufacturing scale and a large installed base. Recurring opportunities arise from sensors, catheters, disposables, replacement implants, service and software associated with durable platforms.
The same breadth creates exposure. Regulatory remediation, recalls and quality failures can interrupt supply or damage trust. Reimbursement changes can slow adoption, while hospital capital constraints affect robotic and navigation platforms. Currency movements matter because international revenue represented 50.2% of FY2026 sales. Tariffs affected FY2026 margins, and the company also faces component availability, cyber, tax and geopolitical risks.
Competition is therapy-specific. Abbott, Boston Scientific and Edwards compete in major cardiovascular categories; Stryker and Johnson & Johnson compete in surgery, spine and neurotechnology; insulin-delivery competitors pressure MiniMed; and imaging or monitoring companies compete in connected hospital workflows. No unsupported company-wide market-share percentage is used here.
| Date | Development | Segment | Significance / source |
| 17 Feb 2026 | Q3 FY2026 results and updated guidance | Company-wide | Confirmed accelerating organic growth; official earnings release |
| 9 Mar 2026 | MiniMed IPO closed | Diabetes / Other | 10% public float changed segment presentation and advanced separation |
| 23 Mar 2026 | OmniaSecure FDA approval | Cardiovascular | Expanded defibrillation lead options for conduction-system pacing |
| 27 Mar 2026 | Stealth AXiS FDA clearance | Neuroscience | Expanded integrated surgical navigation in cranial and ENT |
| 24 Apr 2026 | Cybersecurity incident disclosed | Company-wide | Unauthorized access prompted containment, investigation and remediation |
| 28 Apr 2026 | Stealth AXiS CE Mark announced | Neuroscience | Supported European commercialization for spine and cranial use |
| 3 Jun 2026 | FY2026 results and FY2027 guidance | Company-wide | US$36.364bn sales; 6.75%–7.25% organic FY2027 growth guidance |
| 12 Jun 2026 | Scientia Vascular acquisition completed | Neuroscience | Added neurovascular access products |
| 16 Jul 2026 | SPR Therapeutics acquisition completed | Neuroscience / Neuromodulation | Added temporary peripheral nerve stimulation |
On 3 June 2026, management guided to FY2027 organic revenue growth of 6.75%–7.25% and adjusted diluted EPS of US$5.90–US$5.98. The organic growth range includes a 53rd week and Diabetes revenue for the full fiscal year, while excluding foreign exchange and “Other” revenue. Guidance is a management forecast, not a confirmed result.
Potential growth drivers include pulsed-field ablation, leadless pacing, transcatheter valves, renal denervation, neuromodulation, surgical navigation, Hugo robotics and diabetes automation. Material uncertainties include execution of the MiniMed divestiture, integration of acquisitions, tariffs, foreign exchange, price pressure, reimbursement, clinical and regulatory outcomes, supply resilience, cybersecurity, product quality and litigation or tax exposures.
Medtronic reported US$36.364 billion in net sales for fiscal 2026, the 52-week period ended 24 April 2026. Revenue increased 8.4% as reported and 5.8% organically. The figure is an audited fiscal-year result, not calendar-year 2026 revenue or a management forecast.
Medtronic reported more than 95,000 full-time employees in its FY2026 Form 10-K. The filing states that 43% were based in the United States or Puerto Rico. It does not publish an exact global headcount or a complete breakdown by manufacturing, R&D and commercial function.
Medtronic plc is legally domiciled in Ireland, with its registered office in Galway. Its principal operational headquarters remains in the Minneapolis area of Minnesota, United States. This dual description reflects the corporate structure created after the company completed the Covidien transaction in 2015.
Geoff Martha was Medtronic’s chairman and chief executive officer as of 12 August 2026. Leadership can change, so publication-date context matters. This article verifies the position through Medtronic’s FY2026 filing and investor materials rather than relying on an undated third-party company profile.
At FY2026 year-end, Medtronic’s reportable segments were Cardiovascular, Neuroscience and Medical Surgical. Diabetes remained an operating business but was aggregated with Other after the MiniMed IPO because Medtronic intended to divest its remaining interest. Earlier-year segment presentations may therefore differ.
Cardiovascular was the largest business in FY2026, generating US$13.976 billion in net sales. That equaled approximately 38.4% of consolidated revenue, calculated from audited figures. Its divisions included Cardiac Rhythm & Heart Failure, Structural Heart & Aortic, and Coronary & Peripheral Vascular.
Medtronic recorded US$2.873 billion in GAAP research and development expense in FY2026. That represented approximately 7.9% of net sales, calculated as R&D divided by revenue. Spending covered cardiovascular, neuroscience, surgical, diabetes, robotics, digital and clinical-development programs.
Medtronic describes a global commercial and operating footprint, but its FY2026 Form 10-K does not state one precise, audited country count. The company often uses broad reach language in corporate materials. This article therefore reports U.S. and international revenue without converting marketing descriptions into an exact country statistic.
Major platforms include pacemakers and defibrillators, Micra leadless pacing, heart valves, ablation systems, Symplicity renal denervation, spine and cranial technologies, deep-brain and spinal-cord stimulation, LigaSure surgical instruments, Nellcor monitoring, Hugo robotic-assisted surgery and MiniMed insulin-delivery systems.
Competitors vary by therapy. Important peers include Abbott, Boston Scientific, Stryker, Johnson & Johnson MedTech, Edwards Lifesciences, Becton Dickinson, Baxter, Siemens Healthineers and Philips. No single company competes equally across every Medtronic category, so category-level evidence is more useful than a company-wide market-share claim.
Medtronic plc ordinary shares trade on the New York Stock Exchange under MDT. Investors should distinguish the ticker from the company’s Irish legal domicile and U.S. operational headquarters. Market price and market capitalization change continuously and are therefore not fixed in this publication.
Management’s 3 June 2026 guidance called for 6.75%–7.25% organic revenue growth and US$5.90–US$5.98 adjusted diluted EPS in FY2027. The revenue range includes a 53rd week and full-year Diabetes revenue. Guidance depends on business, currency, regulatory and macroeconomic assumptions and is not guaranteed.
The central Medtronic statistics for 2026 show a company with US$36.364 billion in annual net sales, US$4.801 billion in attributable net income, more than 95,000 employees and US$2.873 billion in R&D expense. Cardiovascular led revenue, while international sales slightly exceeded U.S. sales.
Growth opportunities span ablation, pacing, structural heart, renal denervation, neuroscience, robotics and connected care. Investors and healthcare buyers must balance that pipeline against integration, separation, reimbursement, quality, cybersecurity, supply-chain, tariff and currency risks. Because the MiniMed transaction changed segment reporting, future comparisons should use consistent portfolio definitions.