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REVVITY, INC. (RVTY)

Business Summary

Revvity, Inc. is a leading provider of health science solutions, technologies, expertise and services that deliver complete workflows from discovery to development, and diagnosis to cure, with specialized focus areas in translational multi-omics technologies, biomarker identification, imaging, prediction, screening, detection and diagnosis, and informatics. The company markets its products and services in more than 160 countries and as of December 28, 2025, employed approximately 11,000 employees . Revvity's common stock is listed on the New York Stock Exchange under the symbol RVTY and it is a component of the S&P 500 Index.

Revvity encounters aggressive competition from numerous competitors in many areas of its business, ranging from multinational organizations with a wide range of products to specialized firms with well-established market positions. The company competes on the basis of service level, price, technological innovation, operational efficiency, product differentiation, product availability, quality and reliability, and expects the proportion of large competitors to increase through continued consolidation. No single customer comprises more than 10% of net revenues in the years presented .

Revvity generates revenue through two segments: Life Sciences and Diagnostics. The Life Sciences segment generates revenue from sales of instruments, reagents, software, subscriptions, detection and imaging technologies, extended warranties, training and services in the life sciences market. The Diagnostics segment generates revenue from sales of instruments, solutions, consumables, reagents, and services in the diagnostics market. Revenue from the sale of instruments, reagents, and certain software is recognized at a point in time, while revenue from software as a service, cloud services, subscriptions, and laboratory services and training is recognized over time. The typical length of a contract for service is 12 to 36 months .

The Life Sciences segment provides a comprehensive portfolio of technologies to help life sciences researchers better understand diseases and develop treatments, spanning cell, gene, and protein research. Principal products include reagents such as radiometric detection solutions with over 750 radiochemicals , BioLegend catalog of more than 35,000 SKUs , and instruments like the Opera Phenix Plus high-content screening system and the EnVision multimode plate reader. The segment also offers software including the Signals Research platform and Signals ChemDraw software. Life Sciences Solutions revenue was $1,194.7 million in fiscal year 2025, and Software revenue was $236.4 million .

The Diagnostics segment offers instruments, reagents, assay platforms and software to hospitals, medical labs, clinicians and medical research professionals, with a focus on reproductive health, immunodiagnostics and emerging market diagnostics. Principal products include the DELFIA Xpress screening platform, the Vanadis NIPT offering, the EONIS assay, and the T-SPOT.TB test. The segment also includes the Revvity Omics global laboratory network offering multi-OMIC clinical grade services with testing laboratories in the United States, India, China and the United Kingdom . Immunodiagnostics revenue was $869.9 million in fiscal year 2025, and Reproductive Health revenue was $555.0 million .

During fiscal year 2025, Revvity repurchased 7,264,299 shares of common stock under the Repurchase Program for an aggregate cost of $695.4 million and repurchased 1,245,232 shares of common stock under the New Repurchase Program for an aggregate cost of $120.5 million . The company also paid $32.8 million in dividends and made net payments of $3.0 million on debts . Tariffs enacted and implemented during fiscal year 2025 increased cost of revenue by approximately $25 million , with a net impact on gross margin of approximately $20 million . The company also executed a sale of its United Kingdom pension plan to a third party, with excess plan assets of $2.7 million, net of taxes, reverting to the company .

Total revenue for fiscal year 2025 was $2,856.1 million , compared to $2,755.0 million in fiscal year 2024, an increase of $101.1 million, or 4%. Net income from continuing operations was $239.9 million in fiscal year 2025, compared to $283.1 million in fiscal year 2024. Diluted earnings per share from continuing operations was $2.06 in fiscal year 2025, compared to $2.30 in fiscal year 2024. Net cash provided by operating activities of continuing operations was $589.0 million in fiscal year 2025, compared to $665.0 million in fiscal year 2024.

Business Outlook & Financial Sufficiency

A key growth vector is the advancement of Artificial Intelligence (AI) to further strengthen differentiated offerings and drive internal operating efficiencies, as stated in the company's strategy. The company is in the initial phases of expanding AI into the core functions of its business. New products introduced in fiscal year 2025 include Phenologic.AI software, a module in the Harmony high-content imaging and analysis software that uses a pre-trained deep-learning image-analysis model, and the Living Image Synergy AI in vivo imaging software platform. The Pin-point base editing platform was expanded to include AI-enhanced adenine deaminase editors in collaboration with Profluent.

Another growth vector is the expansion of the product portfolio through both internal research and development and strategic acquisitions. In fiscal year 2025, the company introduced numerous new products across both segments, including the AssayMate workstation, the VivoJect image-guided injection system, the EnVision Nexus multimode plate reader, the NeoLSD 7 Plex MS/MS kit, the Vanadis Core Reagent Cartridge II, and the T-SPOT.Flex interferon-gamma ELISPOT kit. The company's strategy includes augmenting growth in both core business segments through strategic acquisitions and licensing.

The consolidated gross margin decreased 104 basis points in fiscal year 2025 to 54.8% from 55.8% in fiscal year 2024, primarily due to increased tariffs, unfavorable changes in foreign exchange rates, and product mix shift, partially offset by the completion of product rebranding efforts. The consolidated operating margin decreased 10 basis points in fiscal year 2025 due to gross margin headwinds, partially offset by productivity and cost containment initiatives. Restructuring and other costs, net were $55.9 million in fiscal year 2025, primarily including charges associated with workforce reductions and facility consolidations affecting approximately 5% of the workforce .

The company projects an increase in capital expenditures in fiscal year 2026 relative to fiscal year 2025, reflecting a strategic commitment to enhancing digital capabilities, product innovations, and realigning production infrastructure. The company anticipates funding these initiatives through a combination of existing cash reserves and internally generated funds from continuing operations. As of December 28, 2025, the company had cash and cash equivalents of $919.9 million , of which $463.0 million was held by non-U.S. subsidiaries.

Research and development expenses for fiscal year 2025 were $215.8 million , compared to $196.8 million in fiscal year 2024, an increase of $19.0 million, or 10%. Capital expenditures for fiscal year 2025 were $73.5 million , compared to $86.6 million in fiscal year 2024. On October 23, 2025, the Board authorized a new stock repurchase program for an aggregate amount up to $1.0 billion , which will expire on October 22, 2027. As of December 28, 2025, $879.5 million remained available for aggregate repurchases under the New Repurchase Program. The Board declared a quarterly dividend of $0.07 per share for the fourth quarter of fiscal year 2025 and a quarterly dividend of $0.07 per share for the first quarter of fiscal year 2026.

A significant headwind is the impact of tariffs, which increased cost of revenue by approximately $25 million and reduced gross margin by approximately $20 million in fiscal year 2025, primarily affecting products manufactured in Europe for the U.S. market. The company notes that additional tariffs or trade restrictions may materially and adversely affect its results of operations, financial condition, and competitive position. The company also faces risks from global economic and political conditions, including inflation, recession, financial liquidity, interest rates, and currency volatility.

The company faces constraints from changes in government funding and regulations, noting that recently announced and proposed changes in U.S. funding and regulations have created a more cautious spending environment for customers. The company's revenues may be adversely affected if customers delay or reduce purchases as a result of uncertainties surrounding the approval of government or industrial funding proposals or reductions in government funding. Additionally, the company is subject to risks associated with foreign operations, as sales originating outside the United States represented the majority of total revenue in fiscal year 2025 .

Management Sentiments & Priorities

Management's message emphasizes a strategy to develop and deliver innovative products, services and solutions in high-growth markets to address customers' critical needs and drive scientific breakthroughs. Key strategic priorities include strengthening the position within key markets by expanding global product and service offerings, accelerating transformational innovation through internal research and development and third-party collaborations, augmenting growth in both core business segments through strategic acquisitions and licensing, advancing the use of AI to strengthen differentiated offerings and drive internal operating efficiencies, engraining focused operational excellence to improve organizational efficiency and agility, and taking a disciplined approach to capital allocation to support organic investments, pursue mergers and acquisitions and opportunistic share repurchase programs to drive shareholder value. Management states that overall revenue in fiscal year 2025 increased by $101.1 million, or 4%, as compared to fiscal year 2024, and that the company believes its range of product offerings, leading market positions, global scale and financial strength provides a foundation for continued long-term growth, margin expansion and robust cash flow generation.

Financial Details

Total revenue for fiscal year 2025 was $2,856.1 million , compared to $2,755.0 million for fiscal year 2024. Net income from continuing operations was $239.9 million in fiscal year 2025, compared to $283.1 million in fiscal year 2024. Diluted earnings per share from continuing operations was $2.06 in fiscal year 2025, compared to $2.30 in fiscal year 2024. Operating income from continuing operations was $356.6 million in fiscal year 2025, compared to $346.7 million in fiscal year 2024. Gross margin was 54.8% in fiscal year 2025, compared to 55.8% in fiscal year 2024. Net cash provided by operating activities of continuing operations was $589.0 million in fiscal year 2025, compared to $665.0 million in fiscal year 2024. Cash and cash equivalents were $919.9 million as of December 28, 2025, compared to $1,163.4 million as of December 29, 2024. Total debt was $3,220.1 million as of December 28, 2025, compared to $3,150.7 million as of December 29, 2024. Significant one-time items in fiscal year 2025 included restructuring and other costs, net of $55.9 million , asset impairment of $4.8 million , and significant litigation matters and settlements of $12.2 million . In fiscal year 2024, significant items included asset impairment of $22.8 million and acquisition and divestiture-related expenses of $16.3 million . Life Sciences segment revenue was $1,431.1 million with segment operating income of $458.3 million and a segment operating margin of 32.0% . Diagnostics segment revenue was $1,424.9 million with segment operating income of $344.2 million and a segment operating margin of 24.2% .

Risk Factors

The company faces material risk from tariffs, which increased cost of revenue by approximately $25 million and reduced gross margin by approximately $20 million in fiscal year 2025, primarily affecting products manufactured in Europe for the U.S. market, and additional tariffs may materially and adversely affect results. The company has substantial debt of $3,220.1 million as of December 28, 2025, which could impact its ability to obtain future financing and limit other expenditures. The Life Sciences Solutions reporting unit, with a goodwill balance of $4.5 billion at December 28, 2025, had a fair value that exceeded its carrying value by more than 10% but less than 20% as of the November 3, 2025 impairment testing date, and adverse changes in the business could result in impairment. The company is subject to risks from foreign operations, as sales originating outside the United States represented the majority of total revenue in fiscal year 2025 , and changes in foreign currency exchange rates, trade protection measures, and differing tax laws could harm international sales and profitability. The company also faces risk from disruptions in the supply of raw materials from limited or single source suppliers, which could have an adverse effect on business operations.

References

  1. [1] Item 1, Business — Overview
  2. [2] Item 8, Note 2 — Revenue — Major Customer Concentration
  3. [3] Item 8, Note 2 — Revenue — Nature of goods and services
  4. [4] Item 1, Business — Life Sciences Segment — Principal Products
  5. [5] Item 1, Business — Life Sciences Segment — Principal Products
  6. [6] Item 8, Note 2 — Revenue — Disaggregation of revenue
  7. [7] Item 8, Note 2 — Revenue — Disaggregation of revenue
  8. [8] Item 1, Business — Diagnostics Segment — Principal Products
  9. [9] Item 8, Note 2 — Revenue — Disaggregation of revenue
  10. [10] Item 8, Note 2 — Revenue — Disaggregation of revenue
  11. [11] Item 5, Market for Registrant's Common Equity — Stock Repurchases and Dividends
  12. [12] Item 5, Market for Registrant's Common Equity — Stock Repurchases and Dividends
  13. [13] Item 8, Consolidated Statements of Cash Flows
  14. [14] Item 7, MD&A — Liquidity and Capital Resources — Cash Flows
  15. [15] Item 7, MD&A — Consolidated Results of Operations — Cost of Revenue
  16. [16] Item 7, MD&A — Consolidated Results of Operations — Cost of Revenue
  17. [17] Item 8, Note 15 — Employee Benefit Plans — Pension Plans
  18. [18] Item 8, Consolidated Statements of Operations
  19. [19] Item 8, Consolidated Statements of Operations
  20. [20] Item 8, Consolidated Statements of Operations
  21. [21] Item 8, Consolidated Statements of Operations
  22. [22] Item 8, Consolidated Statements of Operations
  23. [23] Item 8, Consolidated Statements of Operations
  24. [24] Item 8, Consolidated Statements of Cash Flows
  25. [25] Item 8, Consolidated Statements of Cash Flows
  26. [26] Item 7, MD&A — Consolidated Results of Operations — Cost of Revenue
  27. [27] Item 7, MD&A — Consolidated Results of Operations — Cost of Revenue
  28. [28] Item 7, MD&A — Consolidated Results of Operations — Selling, General and Administrative Expenses
  29. [29] Item 8, Note 4 — Restructuring and Other Costs
  30. [30] Item 8, Consolidated Balance Sheets
  31. [31] Item 7, MD&A — Liquidity and Capital Resources — Other Potential Liquidity Considerations
  32. [32] Item 8, Consolidated Statements of Operations
  33. [33] Item 8, Consolidated Statements of Operations
  34. [34] Item 8, Consolidated Statements of Cash Flows
  35. [35] Item 8, Consolidated Statements of Cash Flows
  36. [36] Item 5, Market for Registrant's Common Equity — Stock Repurchases and Dividends
  37. [37] Item 5, Market for Registrant's Common Equity — Stock Repurchases and Dividends
  38. [38] Item 5, Market for Registrant's Common Equity — Stock Repurchases and Dividends
  39. [39] Item 5, Market for Registrant's Common Equity — Stock Repurchases and Dividends
  40. [40] Item 7, MD&A — Consolidated Results of Operations — Cost of Revenue
  41. [41] Item 7, MD&A — Consolidated Results of Operations — Cost of Revenue
  42. [42] Item 1A, Risk Factors — Risks Related to our Foreign Operations
  43. [43] Item 7, MD&A — Consolidated Results of Operations — Cost of Revenue
  44. [44] Item 7, MD&A — Consolidated Results of Operations — Cost of Revenue
  45. [45] Item 8, Note 13 — Debt
  46. [46] Item 7, MD&A — Critical Accounting Policies and Estimates — Goodwill
  47. [47] Item 1A, Risk Factors — Risks Related to our Foreign Operations
  48. [48] Item 8, Consolidated Statements of Operations
  49. [49] Item 8, Consolidated Statements of Operations
  50. [50] Item 8, Consolidated Statements of Operations
  51. [51] Item 8, Consolidated Statements of Operations
  52. [52] Item 8, Consolidated Statements of Operations
  53. [53] Item 8, Consolidated Statements of Operations
  54. [54] Item 8, Consolidated Statements of Operations
  55. [55] Item 8, Consolidated Statements of Operations
  56. [56] Item 7, MD&A — Consolidated Results of Operations — Cost of Revenue
  57. [57] Item 7, MD&A — Consolidated Results of Operations — Cost of Revenue
  58. [58] Item 8, Consolidated Statements of Cash Flows
  59. [59] Item 8, Consolidated Statements of Cash Flows
  60. [60] Item 8, Consolidated Balance Sheets
  61. [61] Item 8, Consolidated Balance Sheets
  62. [62] Item 8, Note 13 — Debt
  63. [63] Item 8, Note 13 — Debt
  64. [64] Item 8, Consolidated Statements of Cash Flows
  65. [65] Item 8, Consolidated Statements of Cash Flows
  66. [66] Item 7, MD&A — Consolidated Results of Operations — Selling, General and Administrative Expenses
  67. [67] Item 7, MD&A — Consolidated Results of Operations — Selling, General and Administrative Expenses
  68. [68] Item 7, MD&A — Consolidated Results of Operations — Selling, General and Administrative Expenses
  69. [69] Item 7, MD&A — Reporting Segment Results — Life Sciences
  70. [70] Item 7, MD&A — Reporting Segment Results — Life Sciences
  71. [71] Item 7, MD&A — Reporting Segment Results — Life Sciences
  72. [72] Item 7, MD&A — Reporting Segment Results — Diagnostics
  73. [73] Item 7, MD&A — Reporting Segment Results — Diagnostics
  74. [74] Item 7, MD&A — Reporting Segment Results — Diagnostics

Analysis on 6/21/2026