View ValuationThis company listing is no longer activeThis company may still be operating, however this listing is no longer active.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 향후 성장Future 기준 점검 3/6Revvity (는) 각각 연간 29.3% 및 5.1% 수익과 수익이 증가할 것으로 예상됩니다. EPS는 연간 29.4% 만큼 성장할 것으로 예상됩니다. 자기자본이익률은 3년 후 8.4% 로 예상됩니다.핵심 정보29.3%이익 성장률29.35%EPS 성장률Life Sciences 이익 성장20.2%매출 성장률5.1%향후 자기자본이익률8.39%애널리스트 커버리지Good마지막 업데이트16 Nov 2025최근 향후 성장 업데이트공시 • 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.모든 업데이트 보기Recent updates공시 • 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.공시 • 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.공시 • 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.공시 • 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.공시 • 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, 2025공시 • 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.공시 • Sep 22Revvity, Inc.(NYSE:RVTY) dropped from FTSE All-World Index (USD)Revvity, Inc.(NYSE:RVTY) dropped from FTSE All-World Index (USD)공시 • 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.공시 • 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.공시 • 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.공시 • 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, 2025공시 • 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.공시 • 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.이익 및 매출 성장 예측BIT:1RVTY - 애널리스트 향후 추정치 및 과거 재무 데이터 (USD Millions)날짜매출이익자유현금흐름영업현금흐름평균 애널리스트 수12/31/20273,1045037037811112/31/20262,9323416517371612/31/20252,845241542617169/28/20252,813232497575N/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/A더 보기애널리스트 향후 성장 전망수입 대 저축률: 1RVTY 의 연간 예상 수익 증가율(29.3%)이 saving rate(3%)보다 높습니다.수익 vs 시장: 1RVTY 의 연간 수익(29.3%)이 Italian 시장(11.3%)보다 빠르게 성장할 것으로 예상됩니다.고성장 수익: 1RVTY 의 수입은 향후 3년 동안 상당히 증가할 것으로 예상됩니다.수익 대 시장: 1RVTY 의 수익(연간 5.1%)이 Italian 시장(연간 5.8%)보다 느리게 성장할 것으로 예상됩니다.고성장 매출: 1RVTY 의 수익(연간 5.1%)은 연간 20%보다 느리게 증가할 것으로 예상됩니다.주당순이익 성장 예측향후 자기자본이익률미래 ROE: 1RVTY의 자본 수익률은 3년 후 8.4%로 낮을 것으로 예상됩니다.성장 기업 찾아보기7D1Y7D1Y7D1YPharmaceuticals-biotech 산업의 고성장 기업.View Past Performance기업 분석 및 재무 데이터 상태데이터최종 업데이트 (UTC 시간)기업 분석2025/11/26 19:00종가2025/11/21 00:00수익2025/09/28연간 수익2024/12/29데이터 소스당사의 기업 분석에 사용되는 데이터는 S&P Global Market Intelligence LLC에서 제공됩니다. 아래 데이터는 이 보고서를 생성하기 위해 분석 모델에서 사용됩니다. 데이터는 정규화되므로 소스가 제공된 후 지연이 발생할 수 있습니다.패키지데이터기간미국 소스 예시 *기업 재무제표10년손익계산서현금흐름표대차대조표SEC 양식 10-KSEC 양식 10-Q분석가 컨센서스 추정치+3년재무 예측분석가 목표주가분석가 리서치 보고서Blue Matrix시장 가격30년주가배당, 분할 및 기타 조치ICE 시장 데이터SEC 양식 S-1지분 구조10년주요 주주내부자 거래SEC 양식 4SEC 양식 13D경영진10년리더십 팀이사회SEC 양식 10-KSEC 양식 DEF 14A주요 개발10년회사 공시SEC 양식 8-K* 미국 증권에 대한 예시이며, 비(非)미국 증권에는 해당 국가의 규제 서식 및 자료원을 사용합니다.별도로 명시되지 않는 한 모든 재무 데이터는 연간 기간을 기준으로 하지만 분기별로 업데이트됩니다. 이를 TTM(최근 12개월) 또는 LTM(지난 12개월) 데이터라고 합니다. 자세히 알아보기.분석 모델 및 스노우플레이크이 보고서를 생성하는 데 사용된 분석 모델에 대한 자세한 내용은 당사의 Github 페이지에서 확인하실 수 있습니다. 또한 보고서 활용 방법에 대한 가이드와 YouTube 튜토리얼도 제공합니다.Simply Wall St 분석 모델을 설계하고 구축한 세계적 수준의 팀에 대해 알아보세요.산업 및 섹터 지표산업 및 섹터 지표는 Simply Wall St가 6시간마다 계산하며, 프로세스에 대한 자세한 내용은 Github에서 확인할 수 있습니다.분석가 소스Revvity, Inc.는 34명의 분석가가 다루고 있습니다. 이 중 16명의 분석가가 우리 보고서에 입력 데이터로 사용되는 매출 또는 수익 추정치를 제출했습니다. 분석가의 제출 자료는 하루 종일 업데이트됩니다.분석가기관Catherine Ramsey SchulteBairdCharles ButlerBarclaysLuke SergottBarclays31명의 분석가 더 보기
공시 • 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.
공시 • 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.
공시 • 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.
공시 • 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.
공시 • 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.
공시 • 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
공시 • 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.
공시 • Sep 22Revvity, Inc.(NYSE:RVTY) dropped from FTSE All-World Index (USD)Revvity, Inc.(NYSE:RVTY) dropped from FTSE All-World Index (USD)
공시 • 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.
공시 • 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.
공시 • 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.
공시 • 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
공시 • 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.
공시 • 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.