Analysis: Gilbert Cisneros's sell of RVTY (Revvity, Inc.)
Assessment: Low signal
Routine, advisor-managed trimming of a long-held position, executed as a same-day swap into NXPI, with no committee connection or non-public catalysts.
- Member: Gilbert Cisneros
- Party / state: Democratic-CA
- Chamber: House
- Transaction: Sell
- Amount: $15,001 - $50,000
- Ticker: RVTY
- Company: Revvity, Inc.
- Trade date: 2026-09-09
- Disclosure date: 2026-10-12
- Disclosure lag: 33 days
Executive summary
Research identified the traded asset as Revvity, Inc. (NYSE: RVTY; CIK 0000031791), with a member-reported sale on 2026-09-09 and disclosure on 2026-10-12 (33-day lag). Primary-source context located includes Revvity’s 2025 Form 10-K (filed 2026-02-24) discussing FDA regulation and government-entity sales/contract compliance risk, one company 8-K filed 2026-08-04 reporting Q2 2026 results and a definitive agreement to divest a China immunodiagnostics business, and Federal Register items in 2026 related to FDA medical device classification/exemptions referencing PerkinElmer/related device categories.
Within the member’s user-provided RVTY trading history (10 total transactions), the 2026-09-09 sale occurred after two smaller RVTY sales on 2026-09-03 and 2026-09-04, and was paired with a same-day purchase of NXPI. Primary-source company disclosures in the broader window include an 8-K filed 2026-08-04 with an attached earnings press release stating Revvity entered a definitive agreement to divest its China Immunodiagnostics business and raised full-year guidance. Federal Register documents in 2026 include an FDA order (published 2026-06-11) classifying an SMA newborn screening test system (referencing a PerkinElmer De Novo request) and an FDA order (published 2026-10-06) exempting certain class II clinical toxicology test systems from 510(k) requirements. USAspending recipient profiles show federal award activity for Revvity-related entities (e.g., 'REVVITY HEALTH SCIENCES, INC.'), including obligations attributed to agencies such as HHS and DOD per the profile page, and at least one example DOD maintenance/repair services contract record. Due to a web-search tool result cap encountered during this run, systematic extraction of all Congress.gov legislative/committee activity in the specified windows, full USAspending award lists near the trade date, Regulations.gov open dockets, and contemporaneous news coverage could not be completed.
Timeline
- 2026-06-11 — FDA published order classifying the Spinal Muscular Atrophy newborn screening test system into class II; document references PerkinElmer Inc.'s De Novo request (Eonis SCID-SMA Kit).
- 2026-08-04 — Revvity filed Form 8-K (Items 2.02, 8.01, 9.01) reporting Q2 2026 financial results and attaching press release; press release text includes: entered into definitive agreement to divest China Immunodiagnostics business and raised full-year guidance.
- 2026-09-03 — Member sold RVTY ($1,001-$15,000) per user-provided trading history.
- 2026-09-04 — Member sold RVTY ($1,001-$15,000) per user-provided trading history.
- 2026-09-09 — TRADE UNDER ANALYSIS: Member sold RVTY ($15,001-$50,000) per user-provided trading history.
- 2026-09-09 — Same-day trade: Member purchased NXPI ($15,001-$50,000) per user-provided trading history.
- 2026-09-07 — Congress.gov committee schedule week of Sep 7-13, 2026 shows '0 Meetings' for that week (no meeting data listed for Sep 9, 2026).
- 2026-09-16 — Form 4: insider sale by Tajinder S Vohra (code S) at $140.88/share.
- 2026-09-21 — Form 4: insider sale by Maxwell Krakowiak (code S) at $144.53/share.
- 2026-10-01 — Form 4: insider sale by Anita Gonzales (code S) at $155.48/share.
- 2026-10-06 — FDA published final order exempting certain class II clinical toxicology test systems from 510(k) requirements (subject to limitations).
- 2026-10-12 — Member filed disclosure reporting the 2026-09-09 RVTY sale (per user-provided trade metadata).
Independent analysis of public financial disclosures. Not financial or investment advice.
Sources
- Member IDs for Biographical Directory
- Gilbert Ray Cisneros, Jr. | Congress.gov | Library of Congress
- About Congressional Member Profiles
- Bioguide Search
- Search Tools
- https://www.congress.gov/119/bills/hr858/BILLS-119hr858ih.htm
- All Info - H.R.858 - 119th Congress (2025-2026): REVIVE VI Act | Congress.gov | Library of Congress
- WRITTEN TESTIMONY
- S.2414 - 117th Congress (2021-2022): REVIVE the CCC Act | Congress.gov | Library of Congress
- Variable Renewable Energy: An Introduction | Congress.gov | Library of Congress
- CLIMATE CHANGE AND THE U.S. AGRICULTURE ...
- department of energy user facilities: utilizing the tools of ...
- https://www.congress.gov/115/meeting/house/108525/witnesses/HHRG-115-IF17-TTF-HarmonJ-20180711.pdf
- REVVITY, INC. Form 10-K for the period ended December 28, 2025
- At the inflection point of scientific progress.
- EDGAR Filing Documents for 0000031791-26-000012
- EDGAR Filing Documents for 0000031791-26-000012
- EDGAR Filing Documents for 0000031791-26-000012
- REVVITY, INC. Form 10-K for the period ended December 29, 2024
- From vision to reality: Solving global health challenges together.
- revv-20260705
- Importer of Controlled Substances Application: Revvity, Inc.
- Federal Register :: Revocation of Six Authorizations of Emergency Use of In Vitro Diagnostic Device for Detection and/or Diagnosis of COVID-19; Availability
- Exempt Chemical Preparations Under the Controlled ...
- Federal Register :: 2024 Federal Register Index :: Drug Enforcement Administration
- 05/29/2024 Public Inspection Issue
- Federal Register :: Medical Devices; Immunology and Microbiology Devices; Classification of the Spinal Muscular Atrophy Newborn Screening Test System
- Federal Register :: Medical Devices; Clinical Chemistry and Clinical Toxicology Devices; Classification of the Muscular Dystrophy Newborn Screening Test
- Federal Register :: Importer of Controlled Substances Application: PerkinElmer, Inc.
- Federal Register :: Importer of Controlled Substances Application: Perkinelmer, Inc.
- Federal Register :: Medical Devices; Exemptions From Premarket Notification: Class II Devices; Certain Clinical Toxicology Test Systems
- REVVITY INC | Federal Award Recipient Profile | USAspending
- REVVITY HEALTH SCIENCES, INC. | Federal Award Recipient ...
- REVVITY SIGNALS SOFTWARE, INC. | Federal Award Recipient ...
- CONTRACT to REVVITY HEALTH SCIENCES, INC. | USAspending
- CONTRACT to REVVITY INC | USAspending
- PERKINELMER U.S. LLC | Federal Award Recipient Profile | USAspending
- PERKINELMER U.S. LLC | Federal Award Recipient Profile
- PERKINELMER JAPAN G.K. | Federal Award Recipient Profile | USAspending
- CONTRACT to PERKINELMER JAPAN G.K. | USAspending
- CONTRACT to PERKINELMER U.S. LLC | USAspending
- Notice of Request for Public Comments on Section 232 ...
- Patent Term Extension Application for EVENITY (romosozumab-aqqg), Patent No. 7,592,429
- Federal Register, Volume 89 Issue 207 (Friday, October 25, 2024)
- Notice of Approval of Product Under Voucher: Rare Pediatric Disease Priority Review Voucher
- Patent Term Extension Application for VUMERITY (diroximel fumarate), Patent No. 10,080,733
- Committee Schedule for the Week of September 7 - 13, 2026 | Congress.gov | Library of Congress
- Congress, week of September 7, 2026 | Civitas