Access to Pediatric Technologies Act of 2025
Summary
What This Bill Does
The Access to Pediatric Technologies Act creates a Medicare payment pathway for qualifying pediatric technologies that lack national relative value units under the physician fee schedule. Starting with technologies furnished on or after January 1, 2026, the HHS Secretary must establish RVUs when a manufacturer requests them and supplies information verifying pediatric eligibility and supporting payment valuation. The Secretary must use the physician fee schedule methodology and available data such as contractor pricing, claims, time-and-motion studies, invoices, and other rate-setting information. Requests received on or before May 1 must be handled in that year's physician fee schedule rulemaking; later requests move to the following year's process. Qualifying devices must be Medicare-covered, FDA approved, cleared, or authorized, described by a temporary Level I HCPCS code for emerging technologies, services, or procedures, and predominantly used in pediatric procedures or specifically designed for safe and effective pediatric use. The bill does not itself require Medicare coverage or change medical-necessity rules.
Who Benefits and How
Pediatric medical device manufacturers benefit from a defined process to obtain national RVUs for emerging pediatric technologies. Children needing specialized procedures benefit if national payment values make pediatric technologies easier for clinicians to furnish. Pediatric specialists benefit from more predictable Medicare physician fee schedule valuation for qualifying devices and procedures. Hospitals and outpatient practices benefit when national RVUs replace inconsistent contractor pricing for pediatric technologies.
Who Bears the Burden and How
CMS must evaluate manufacturer requests, verify qualifying pediatric technology status, and establish RVUs through annual rulemaking. Manufacturers must submit pricing, claims, time-and-motion, invoice, or other relevant data to support valuation. Medicare contractors must adjust payment systems once national RVUs are established. Federal taxpayers and Medicare may face higher spending when national payment values increase access to qualifying technologies.
Key Provisions
- Requires Medicare to establish national RVUs for qualifying pediatric technologies upon manufacturer request.
- Applies to qualifying pediatric technologies furnished on or after January 1, 2026.
- Creates May 1 timing rules for same-year or following-year physician fee schedule rulemaking.
- Limits qualifying technologies to covered, FDA-authorized, temporary-HCPCS pediatric devices without changing coverage or medical-necessity rules.
Evidence Chain:
This summary is generated from the full bill text using AI analysis. Expand "Detailed Analysis" below for identified beneficiaries/burden bearers with clause-level evidence links.
At a Glance
What This Bill Does
Requires Medicare, upon manufacturer request, to establish national physician fee schedule relative value units for qualifying pediatric technologies furnished on or after January 1, 2026, using available pricing, claims, time-and-motion, invoice, and other data, with same-year rulemaking for requests received by May 1.
Key Policy Areas
Medicare, Medical Devices, Pediatric Care
Primary Purpose
Requires Medicare, upon manufacturer request, to establish national physician fee schedule relative value units for qualifying pediatric technologies furnished on or after January 1, 2026, using available pricing, claims, time-and-motion, invoice, and other data, with same-year rulemaking for requests received by May 1.
Policy Domains
Resolution provisions
Identified Gains
- Pediatric medical device manufacturers
- Children needing specialized procedures
- Pediatric specialists
- Hospitals
Identified Costs
- Centers for Medicare & Medicaid Services
- Medical device manufacturers
- Medicare contractors
- Medicare program
Sponsors
Legislative Progress
In CommitteeMr. Joyce of Pennsylvania (for himself and Mrs. Trahan) introduced …
Referred to the Committee on Energy and Commerce, and in …
Introduced in House
Stakeholder Effects
cui bono?How this legislation distributes effects. Mention counts reflect frequency, not effect magnitude.
Medical device manufacturers, Pediatric medical device manufacturers
Positive-direction: Pediatric medical device manufacturers
Negative-direction: Medical device manufacturers
Bill Structure & Actor Mappings
Who is "The Secretary" in each section?
We use a combination of our own taxonomy and classification in addition to large language models to assess meaning and potential beneficiaries. High confidence means strong textual evidence. Always verify with the original bill text.
Learn more about our methodology