The short answer. SBIR and STTR authority lapsed on October 1, 2025 and was restored by Public Law 119-83, approved April 13, 2026, through September 30, 2031. NIH Phase I awards go up to $323,090 and Phase II up to $2,153,927 under SBA guidelines. The next NIH standard due date is January 5, 2027; the next NSF full proposal deadline is November 4, 2026.
What happened in 2025 and 2026
- October 1, 2025: authority expired. NIH withdrew its SBIR and STTR funding opportunities; active awards continued.
- NIH held no receipt date in April 2026.
- April 13, 2026: the Small Business Innovation and Economic Security Act (Public Law 119-83) extended the programs to September 30, 2031. It allows unspent FY2026 funds to be used in FY2027, creates Strategic Breakthrough Phase II awards of up to $30,000,000 with at least 100 percent matching funds, requires agencies to cap proposals per company from FY2027, and adds research security checks.
- May 2026: NIH posted new parent announcements (SBIR PA-27-100, STTR PA-27-102); NSF relaunched with solicitation NSF 26-510.
NIH in 2026 and 2027
| Item | Figure |
|---|---|
| Phase I (SBA guideline) | $323,090 |
| Phase II (SBA guideline) | $2,153,927 |
| Commercialization Readiness Pilot | $4,191,495, up to 3 years |
| Standard due dates (PA-27-100) | September 5, 2026; January 5, 2027; April 5, 2027 |
| Applications per company | Up to 9 new and resubmitted Phase I, Fast-Track and Direct to Phase II applications per fiscal year |
| Late applications | Not accepted |
For device companies, NIBIB lists interest in bionics, medical devices, medical simulators, robotics, imaging and point-of-care technologies. It accepts Commercialization Readiness Pilot projects but not Phase IIB. Fast-Track lets you apply for Phase I and Phase II in one application.
NSF
| Item | Figure |
|---|---|
| Phase I | Up to $305,000, 6 to 18 months |
| Phase II | Up to $1,250,000, typically 24 months |
| Next full proposal deadlines | November 4, 2026; March 4, 2027; July 7, 2027 |
| First step | An invited Project Pitch; at most two pitches per company per 12 months |
How much work can go to an outside engineering firm
| Program and phase | Minimum done by the small business | Third parties |
|---|---|---|
| SBIR Phase I | Two thirds (67%) of the research effort | Generally not more than 33% |
| SBIR Phase II | One half (50%) | Up to 50% |
| STTR | At least 40% | At least 30% by one partner research institution |
PA-27-100 also states that applications involving foreign subawards or subcontracts will be deemed noncompliant. If grant money will pay for outside engineering, confirm where the work will be performed and which legal entity performs it with your program officer before you name a partner in the application.
Planning tips
- Use Phase I to prove feasibility with a defined prototype and test plan; reviewers fund evidence, not ambition.
- Budget engineering within the subcontract limits and keep the core research in your company.
- Ask NIH program staff early which institute fits your device, and check that institute’s budget limits in the announcement.
Lisa Voronkova talked about the risks that sink medical device products on the Grant Engine roundtable.
Sources
- Public Law 119-83, Small Business Innovation and Economic Security Act
- NIH NOT-OD-26-006: expiration of SBIR and STTR authority
- NIH PA-27-100, SBIR parent announcement
- NIH SEED: understanding SBIR and STTR
- SBIR.gov: about
- NIH: institute funding considerations
- SBA SBIR/STTR Policy Directive, May 2023
- NSF 26-510 solicitation
What OVA does here, and where our responsibility ends
OVA Solutions is a medical device engineering group working under an ISO 13485:2016 certified quality system: 62 engineers, 220 devices developed, $125 per hour, offices in New York, Florida, the United Kingdom, Estonia and Ukraine. We design electronics, firmware and mechanics and take a device from concept to design for manufacturing. We are not a regulatory consultancy and not a contract manufacturer: the regulatory strategy and the submission stay with you or your regulatory consultant.
More from OVA: what medical device development costs, how to choose a development firm, answers from Lisa Voronkova, our quality system.
Updated on October 8, 2026.