View ValuationThis company listing is no longer activeThis company may still be operating, however this listing is no longer active. Find out why through their latest events.See Latest EventsRevvity 将来の成長Future 基準チェック /36Revvity利益と収益がそれぞれ年間29.3%と5.1%増加すると予測されています。EPS は年間 増加すると予想されています。自己資本利益率は 3 年後に8.4% 29.4%なると予測されています。主要情報29.3%収益成長率29.35%EPS成長率Life Sciences 収益成長20.2%収益成長率5.1%将来の株主資本利益率8.39%アナリストカバレッジGood最終更新日16 Nov 2025今後の成長に関する最新情報お知らせ • Jul 29Revvity, Inc. Updates Earnings Guidance for the Full Year Ending December 28, 2025Revvity, Inc. updated earnings guidance for the full year ending December 28, 2025. The company is raising its revenue guidance to a range of $2.84 billion to $2.88 billion to reflect recent changes in foreign currency exchange rates and assumes 2% to 4% organic growth.すべての更新を表示Recent updatesお知らせ • Nov 10Revvity, Inc. (NYSE:RVTY) entered into a definitive agreement to acquire Advanced Chemistry Development, Inc.Revvity, Inc. (NYSE:RVTY) entered into a definitive agreement to acquire Advanced Chemistry Development, Inc. on November 10, 2025. The transaction is expected to close late in Q4 2025.Reported Earnings • Oct 28Third quarter 2025 earnings released: EPS: US$0.41 (vs US$0.76 in 3Q 2024)Third quarter 2025 results: EPS: US$0.41 (down from US$0.76 in 3Q 2024). Revenue: US$698.9m (up 2.2% from 3Q 2024). Net income: US$47.2m (down 49% from 3Q 2024). Profit margin: 6.8% (down from 14% in 3Q 2024). Revenue is forecast to grow 5.1% p.a. on average during the next 3 years, compared to a 9.6% growth forecast for the Life Sciences industry in Europe.お知らせ • Oct 27+ 1 more updateRevvity, Inc. (NYSE:RVTY) announces an Equity Buyback for $1,000 million worth of its shares.Revvity, Inc. (NYSE:RVTY) announces a share repurchase program. Under the program, the company will repurchase up to $1,000 million worth of its own shares. The program is valid for 2 years.お知らせ • Oct 25Revvity, Inc. Appoints Anita Gonzales as Vice President and Chief Accounting Officer, Effective October 23, 2025On October 23, 2025, the Board of Directors of Revvity, Inc. appointed Anita Gonzales, the Company’s Vice President and Controller, to serve as its Vice President and Chief Accounting Officer, effective October 23, 2025. Mrs. Gonzales, 49, has served as the Company’s Vice President and Controller since May 2023, having joined the Company as Senior Director of Integration and Controllership Initiatives in March 2021. Prior to joining the Company, Mrs. Gonzales was at General Electric Company (“GE”) for ten years. During her tenure at GE, Mrs. Gonzales was Director of Audit and Advisory Practices Corporate division from 2016 to 2021, with responsibility for technical accounting and audit standards of the Corporate Audit Staff. Before that, Mrs. Gonzales held executive roles at GE Aviation including Global Controller-Commercial Engines. Earlier in her career, she held roles of increasing responsibility, up to Senior Manager, at PricewaterhouseCoopers. Mrs. Gonzales holds Master of Public Accounting and Bachelor of Business Administration degrees from the University of Texas at Austin and is a Certified Public Accountant.お知らせ • Oct 24Revvity Board Declares Quarterly Dividend, Payable on February 6, 2026The Board of Directors of Revvity, Inc. declared a regular quarterly dividend of $0.07 per share of common stock. This dividend is payable on February 6, 2026 to all shareholders of record at the close of business on January 16, 2026.お知らせ • Oct 06Revvity, Inc. to Report Q3, 2025 Results on Oct 27, 2025Revvity, Inc. announced that they will report Q3, 2025 results Pre-Market on Oct 27, 2025お知らせ • Sep 30Revvity, Inc. Unveils New AI Software Offering to Transform Preclinical Imaging AnalysisRevvity, Inc. announced the launch of its Living Image Synergy AI multimodal analysis software for in vivo imaging researchers. The solution provides a unified platform with AI capabilities for seamless data analysis across optical, microCT, ultrasound, and other modalities--reducing data inconsistencies, streamlining workflows, increasing throughput, and enhancing reproducibility, all with the intention of accelerating scientific discovery. The Living Image Synergy AI software centralizes analysis with a goal of eliminating the need for separate tools and enabling seamless correlation of datasets. Revvity developed this unified approach to help researchers uncover biological insights that might otherwise remain hidden when using isolated systems. To further streamline workflows, the software features intuitive co-registration tools and automated processes that reduce manual tasks and analysis time. Advanced AI algorithms automate image segmentation and region-of-interest (ROI) quantification--traditionally labor-intensive and variable steps in imaging analysis. This helps support high-throughput analysis and allows researchers to more efficiently monitor disease progression and assess therapeutic efficacy with greater accuracy and statistical confidence.お知らせ • Sep 22Revvity, Inc.(NYSE:RVTY) dropped from FTSE All-World Index (USD)Revvity, Inc.(NYSE:RVTY) dropped from FTSE All-World Index (USD)お知らせ • Aug 07Revvity Launches Innovative Reagent Technology to Accelerate Development of Next-Generation Targeted TherapeuticsRevvity, Inc. announced the launch of pHSense™? reagents, a powerful technology designed to advance internalization studies in drug discovery. pHSense reagents are designed for high-throughput, plate-based workflows and intended for researchers studying G protein-coupled receptors (GPCRs) or antibody-drug conjugates (ADCs). They offer a scalable, accurate, and easy-to-implement solution for monitoring antibody, ADC, or receptor internalization. Developed for use with standard plate readers, pHSense reagents combine a pH-sensitive dye and a time-resolved fluorescence (TRF) readout to allow for the delivery of robust kinetics of internalization and high signal-to- background--even at low endogenous receptor expression levels. Fully compatible with Revvity's multimode detection platforms, pHSense reagents have the potential to significantly enhance detection capability while simplifying integration into existing drug discovery workflows. By enabling more efficient screening and characterization of promising therapeutic candidates, pHSense reagents can help researchers accelerate preclinical development timelines, potentially reducing overall development costs and contributing to more efficient advancement of candidates toward clinical evaluation. With a growing focus on receptor trafficking in drug development and increasing demand for accurate, high-throughput tools, pHSense reagents offer support for emerging trends in oncology and precision medicine, particularly in ADC development. The innovative design focused on addressing major limitations of current offerings such as low throughput and suboptimal signal-to-noise ratios.お知らせ • Jul 29Revvity, Inc. Updates Earnings Guidance for the Full Year Ending December 28, 2025Revvity, Inc. updated earnings guidance for the full year ending December 28, 2025. The company is raising its revenue guidance to a range of $2.84 billion to $2.88 billion to reflect recent changes in foreign currency exchange rates and assumes 2% to 4% organic growth.お知らせ • Jul 25Revvity, Inc. Declares Quarterly Dividend, Payable on November 7, 2025The Board of Directors of Revvity, Inc. declared a regular quarterly dividend of $0.07 per share of common stock. This dividend is payable on November 7, 2025 to all shareholders of record at the close of business on October 17, 2025.お知らせ • Jul 07Revvity, Inc. to Report Q2, 2025 Results on Jul 28, 2025Revvity, Inc. announced that they will report Q2, 2025 results Pre-Market on Jul 28, 2025お知らせ • Jun 02Revvity, Inc. Introduces New IVD Reference Standards for Monitoring Oncology Diagnostic Testing WorkflowsRevvity, Inc. announced the launch of three Mimix reference standards for IVD use, designed for monitoring of next-generation sequencing (NGS) or droplet digital polymerase chain reacting (ddPCR) assays designed to detect somatic mutations in genomic DNA (gDNA) from human samples for IVD use. These cell line-derived reference standards have undergone appropriate design controls to meet U.S. Food and Drug Administration (FDA) regulatory requirements, which helps laboratories integrate them into existing workflows to support monitoring test performance, assay variation, and to help identify increases in random or systemic errors. Offering the Mimix reference standards for IV D indicates the products have been developed and manufactured in accordance with applicable quality system requirements allowing for improved reliability and precision of these reference standards. The three Mimix reference standards cover key cancer testing applications, which include: Mimix OncoSpan FFPE Reference Standard IVD (HD832-IVD); Mimix OncoSpan gDNA Reference Standard IVD (HD 827-IVD); Mimix Myeloid Cancer Panel, gDNA Reference Standard IVD.お知らせ • May 20Revvity's EUROIMMUN Unveils New Fully Automated Instrument for Specialty TestingRevvity, Inc. announced the launch of its new IDS i20™? analytical random access platform from EUROIMMUN, enabling full automation of chemiluminescence immunoassays (ChLIA). The IDS i20 platform is a CE marked and FDA listed device that allows laboratories to consolidate multiple specialty tests on a unique single instrument with greater reagent capacity and higher test throughput compared to existing offerings. The highly versatile IDS i20 instrument allows users to simultaneously run 20 analytes from six diagnostic specialties on a single device. These specialties include endocrinology, allergy, autoimmune and infectious disease testing, testing for Alzheimer's disease and therapeutic drug monitoring. While specialty assays in these diagnostic areas tend to be processed manually or with semi-automated, low-throughput analyzers, the IDS i20 platform offers labs a new means of more flexible, fully automated ChLIA processing. With the ability to process up to 140 tests per hour (assay dependent), the IDS i20 instrument is the latest addition to the well-established IDS i-device series, built on more than 50 years of experience in medical device design and innovation. The IDS i20 platform features new software offering a high degree of adaptability and scalability, along with a superior graphical user interface that meets the latest standards of ergonomics, usability and cybersecurity. Continuous loading of samples and reagents as well as the integrated cooling of ready-to-use reagent cartridges allow for non-stop operation of the system - maximizing efficiency and minimizing hands-on time.業績と収益の成長予測BIT:1RVTY - アナリストの将来予測と過去の財務データ ( )USD Millions日付収益収益フリー・キャッシュフロー営業活動によるキャッシュ平均アナリスト数12/31/20273,1045037037811112/31/20262,9323416517371612/31/20252,845241542617169/28/20252,813232497575N/A6/29/20252,798279503585N/A3/30/20252,770296524609N/A12/29/20242,755283542628N/A9/29/20242,722258564651N/A6/30/20242,708197383469N/A3/31/20242,72618397175N/A12/31/20232,7511801091N/A10/1/20232,796213-5034N/A7/2/20232,837250153227N/A4/2/20233,024353380460N/A1/1/20233,312513594680N/A10/2/20223,599599790876N/A7/3/20223,7486379321,030N/A4/3/20223,4836941,1221,220N/A1/2/20223,8288891,3251,411N/A10/3/20214,1551,0861,4781,557N/A7/4/20214,2571,1551,3801,455N/A4/4/20214,4381,0741,2341,306N/A1/3/20212,663631829892N/A10/4/20203,234412545625N/A7/5/20202,977294444521N/A4/5/20202,887226352429N/A12/29/20192,884228282363N/A9/29/20192,835235217308N/A6/30/20192,802251N/A294N/A3/31/20192,783247N/A320N/A12/30/20182,778237N/A311N/A9/30/20182,663128N/A280N/A7/1/20182,543149N/A245N/A4/1/20182,387147N/A220N/A12/31/20172,257157N/A288N/A10/1/20172,182258N/A309N/A7/2/20172,142215N/A324N/A4/2/20172,132210N/A372N/A1/1/20172,116216N/A351N/A10/2/20161,999198N/A327N/A7/3/20162,048199N/A314N/A4/3/20162,076190N/A281N/A1/3/20162,105189N/A287N/A10/4/20152,263176N/A258N/A6/28/20152,241164N/A261N/A3/29/20152,234167N/A252N/A12/28/20142,070130N/A282N/Aもっと見るアナリストによる今後の成長予測収入対貯蓄率: 1RVTYの予測収益成長率 (年間29.3% ) は 貯蓄率 ( 3% ) を上回っています。収益対市場: 1RVTYの収益 ( 29.3% ) はItalian市場 ( 11.3% ) よりも速いペースで成長すると予測されています。高成長収益: 1RVTYの収益は今後 3 年間で 大幅に 増加すると予想されています。収益対市場: 1RVTYの収益 ( 5.1% ) Italian市場 ( 5.8% ) よりも低い成長が予測されています。高い収益成長: 1RVTYの収益 ( 5.1% ) 20%よりも低い成長が予測されています。一株当たり利益成長率予想将来の株主資本利益率将来のROE: 1RVTYの 自己資本利益率 は、3年後には低くなると予測されています ( 8.4 %)。成長企業の発掘7D1Y7D1Y7D1YPharmaceuticals-biotech 業界の高成長企業。View Past Performance企業分析と財務データの現状データ最終更新日（UTC時間）企業分析2025/11/26 20:13終値2025/11/21 00:00収益2025/09/28年間収益2024/12/29データソース企業分析に使用したデータはS&P Global Market Intelligence LLC のものです。本レポートを作成するための分析モデルでは、以下のデータを使用しています。データは正規化されているため、ソースが利用可能になるまでに時間がかかる場合があります。パッケージデータタイムフレーム米国ソース例会社財務10年損益計算書キャッシュ・フロー計算書貸借対照表SECフォーム10-KSECフォーム10-Qアナリストのコンセンサス予想+プラス3年予想財務アナリストの目標株価アナリストリサーチレポートBlue Matrix市場価格30年株価配当、分割、措置ICEマーケットデータSECフォームS-1所有権10年トップ株主インサイダー取引SECフォーム4SECフォーム13Dマネジメント10年リーダーシップ・チーム取締役会SECフォーム10-KSECフォームDEF 14A主な進展10年会社からのお知らせSECフォーム8-K* 米国証券を対象とした例であり、非米国証券については、同等の規制書式および情報源を使用。特に断りのない限り、すべての財務データは1年ごとの期間に基づいていますが、四半期ごとに更新されます。これは、TTM（Trailing Twelve Month）またはLTM（Last Twelve Month）データとして知られています。詳細はこちら。分析モデルとスノーフレーク本レポートを生成するために使用した分析モデルの詳細は当社のGithubページでご覧いただけます。また、レポートの使用方法に関するガイドやYoutubeのチュートリアルも掲載しています。シンプリー・ウォールストリート分析モデルを設計・構築した世界トップクラスのチームについてご紹介します。業界およびセクターの指標私たちの業界とセクションの指標は、Simply Wall Stによって6時間ごとに計算されます。アナリスト筋Revvity, Inc. 16 これらのアナリストのうち、弊社レポートのインプットとして使用した売上高または利益の予想を提出したのは、 。アナリストの投稿は一日中更新されます。34 アナリスト機関Catherine Ramsey SchulteBairdCharles ButlerBarclaysLuke SergottBarclays31 その他のアナリストを表示
お知らせ • Jul 29Revvity, Inc. Updates Earnings Guidance for the Full Year Ending December 28, 2025Revvity, Inc. updated earnings guidance for the full year ending December 28, 2025. The company is raising its revenue guidance to a range of $2.84 billion to $2.88 billion to reflect recent changes in foreign currency exchange rates and assumes 2% to 4% organic growth.
お知らせ • Nov 10Revvity, Inc. (NYSE:RVTY) entered into a definitive agreement to acquire Advanced Chemistry Development, Inc.Revvity, Inc. (NYSE:RVTY) entered into a definitive agreement to acquire Advanced Chemistry Development, Inc. on November 10, 2025. The transaction is expected to close late in Q4 2025.
Reported Earnings • Oct 28Third quarter 2025 earnings released: EPS: US$0.41 (vs US$0.76 in 3Q 2024)Third quarter 2025 results: EPS: US$0.41 (down from US$0.76 in 3Q 2024). Revenue: US$698.9m (up 2.2% from 3Q 2024). Net income: US$47.2m (down 49% from 3Q 2024). Profit margin: 6.8% (down from 14% in 3Q 2024). Revenue is forecast to grow 5.1% p.a. on average during the next 3 years, compared to a 9.6% growth forecast for the Life Sciences industry in Europe.
お知らせ • Oct 27+ 1 more updateRevvity, Inc. (NYSE:RVTY) announces an Equity Buyback for $1,000 million worth of its shares.Revvity, Inc. (NYSE:RVTY) announces a share repurchase program. Under the program, the company will repurchase up to $1,000 million worth of its own shares. The program is valid for 2 years.
お知らせ • Oct 25Revvity, Inc. Appoints Anita Gonzales as Vice President and Chief Accounting Officer, Effective October 23, 2025On October 23, 2025, the Board of Directors of Revvity, Inc. appointed Anita Gonzales, the Company’s Vice President and Controller, to serve as its Vice President and Chief Accounting Officer, effective October 23, 2025. Mrs. Gonzales, 49, has served as the Company’s Vice President and Controller since May 2023, having joined the Company as Senior Director of Integration and Controllership Initiatives in March 2021. Prior to joining the Company, Mrs. Gonzales was at General Electric Company (“GE”) for ten years. During her tenure at GE, Mrs. Gonzales was Director of Audit and Advisory Practices Corporate division from 2016 to 2021, with responsibility for technical accounting and audit standards of the Corporate Audit Staff. Before that, Mrs. Gonzales held executive roles at GE Aviation including Global Controller-Commercial Engines. Earlier in her career, she held roles of increasing responsibility, up to Senior Manager, at PricewaterhouseCoopers. Mrs. Gonzales holds Master of Public Accounting and Bachelor of Business Administration degrees from the University of Texas at Austin and is a Certified Public Accountant.
お知らせ • Oct 24Revvity Board Declares Quarterly Dividend, Payable on February 6, 2026The Board of Directors of Revvity, Inc. declared a regular quarterly dividend of $0.07 per share of common stock. This dividend is payable on February 6, 2026 to all shareholders of record at the close of business on January 16, 2026.
お知らせ • Oct 06Revvity, Inc. to Report Q3, 2025 Results on Oct 27, 2025Revvity, Inc. announced that they will report Q3, 2025 results Pre-Market on Oct 27, 2025
お知らせ • Sep 30Revvity, Inc. Unveils New AI Software Offering to Transform Preclinical Imaging AnalysisRevvity, Inc. announced the launch of its Living Image Synergy AI multimodal analysis software for in vivo imaging researchers. The solution provides a unified platform with AI capabilities for seamless data analysis across optical, microCT, ultrasound, and other modalities--reducing data inconsistencies, streamlining workflows, increasing throughput, and enhancing reproducibility, all with the intention of accelerating scientific discovery. The Living Image Synergy AI software centralizes analysis with a goal of eliminating the need for separate tools and enabling seamless correlation of datasets. Revvity developed this unified approach to help researchers uncover biological insights that might otherwise remain hidden when using isolated systems. To further streamline workflows, the software features intuitive co-registration tools and automated processes that reduce manual tasks and analysis time. Advanced AI algorithms automate image segmentation and region-of-interest (ROI) quantification--traditionally labor-intensive and variable steps in imaging analysis. This helps support high-throughput analysis and allows researchers to more efficiently monitor disease progression and assess therapeutic efficacy with greater accuracy and statistical confidence.
お知らせ • Sep 22Revvity, Inc.(NYSE:RVTY) dropped from FTSE All-World Index (USD)Revvity, Inc.(NYSE:RVTY) dropped from FTSE All-World Index (USD)
お知らせ • Aug 07Revvity Launches Innovative Reagent Technology to Accelerate Development of Next-Generation Targeted TherapeuticsRevvity, Inc. announced the launch of pHSense™? reagents, a powerful technology designed to advance internalization studies in drug discovery. pHSense reagents are designed for high-throughput, plate-based workflows and intended for researchers studying G protein-coupled receptors (GPCRs) or antibody-drug conjugates (ADCs). They offer a scalable, accurate, and easy-to-implement solution for monitoring antibody, ADC, or receptor internalization. Developed for use with standard plate readers, pHSense reagents combine a pH-sensitive dye and a time-resolved fluorescence (TRF) readout to allow for the delivery of robust kinetics of internalization and high signal-to- background--even at low endogenous receptor expression levels. Fully compatible with Revvity's multimode detection platforms, pHSense reagents have the potential to significantly enhance detection capability while simplifying integration into existing drug discovery workflows. By enabling more efficient screening and characterization of promising therapeutic candidates, pHSense reagents can help researchers accelerate preclinical development timelines, potentially reducing overall development costs and contributing to more efficient advancement of candidates toward clinical evaluation. With a growing focus on receptor trafficking in drug development and increasing demand for accurate, high-throughput tools, pHSense reagents offer support for emerging trends in oncology and precision medicine, particularly in ADC development. The innovative design focused on addressing major limitations of current offerings such as low throughput and suboptimal signal-to-noise ratios.
お知らせ • Jul 29Revvity, Inc. Updates Earnings Guidance for the Full Year Ending December 28, 2025Revvity, Inc. updated earnings guidance for the full year ending December 28, 2025. The company is raising its revenue guidance to a range of $2.84 billion to $2.88 billion to reflect recent changes in foreign currency exchange rates and assumes 2% to 4% organic growth.
お知らせ • Jul 25Revvity, Inc. Declares Quarterly Dividend, Payable on November 7, 2025The Board of Directors of Revvity, Inc. declared a regular quarterly dividend of $0.07 per share of common stock. This dividend is payable on November 7, 2025 to all shareholders of record at the close of business on October 17, 2025.
お知らせ • Jul 07Revvity, Inc. to Report Q2, 2025 Results on Jul 28, 2025Revvity, Inc. announced that they will report Q2, 2025 results Pre-Market on Jul 28, 2025
お知らせ • Jun 02Revvity, Inc. Introduces New IVD Reference Standards for Monitoring Oncology Diagnostic Testing WorkflowsRevvity, Inc. announced the launch of three Mimix reference standards for IVD use, designed for monitoring of next-generation sequencing (NGS) or droplet digital polymerase chain reacting (ddPCR) assays designed to detect somatic mutations in genomic DNA (gDNA) from human samples for IVD use. These cell line-derived reference standards have undergone appropriate design controls to meet U.S. Food and Drug Administration (FDA) regulatory requirements, which helps laboratories integrate them into existing workflows to support monitoring test performance, assay variation, and to help identify increases in random or systemic errors. Offering the Mimix reference standards for IV D indicates the products have been developed and manufactured in accordance with applicable quality system requirements allowing for improved reliability and precision of these reference standards. The three Mimix reference standards cover key cancer testing applications, which include: Mimix OncoSpan FFPE Reference Standard IVD (HD832-IVD); Mimix OncoSpan gDNA Reference Standard IVD (HD 827-IVD); Mimix Myeloid Cancer Panel, gDNA Reference Standard IVD.
お知らせ • May 20Revvity's EUROIMMUN Unveils New Fully Automated Instrument for Specialty TestingRevvity, Inc. announced the launch of its new IDS i20™? analytical random access platform from EUROIMMUN, enabling full automation of chemiluminescence immunoassays (ChLIA). The IDS i20 platform is a CE marked and FDA listed device that allows laboratories to consolidate multiple specialty tests on a unique single instrument with greater reagent capacity and higher test throughput compared to existing offerings. The highly versatile IDS i20 instrument allows users to simultaneously run 20 analytes from six diagnostic specialties on a single device. These specialties include endocrinology, allergy, autoimmune and infectious disease testing, testing for Alzheimer's disease and therapeutic drug monitoring. While specialty assays in these diagnostic areas tend to be processed manually or with semi-automated, low-throughput analyzers, the IDS i20 platform offers labs a new means of more flexible, fully automated ChLIA processing. With the ability to process up to 140 tests per hour (assay dependent), the IDS i20 instrument is the latest addition to the well-established IDS i-device series, built on more than 50 years of experience in medical device design and innovation. The IDS i20 platform features new software offering a high degree of adaptability and scalability, along with a superior graphical user interface that meets the latest standards of ergonomics, usability and cybersecurity. Continuous loading of samples and reagents as well as the integrated cooling of ready-to-use reagent cartridges allow for non-stop operation of the system - maximizing efficiency and minimizing hands-on time.