Large Flat Panel Detector (LFPD )
Closed Pre-Solicitation Posted
- Solicitation number
- CDRH-2026-133668
- Agency
- FDA Office of Acquisition and Grant Services Food and Drug Administration, Department of Health and Human Services
- Responses due
- Set-aside
- No set-aside
Opportunity facts
- NAICS code
- 334510 Electromedical and Electrotherapeutic Apparatus Manufacturing
- Place of performance
- Silver Spring, Maryland 20993, United States
- Points of contact
-
- Freshta Javid freshta.javid@fda.hhs.gov (301) 796-0385
Notice details come from SAM.gov. Updated .
About this opportunity
The FDA Office of Acquisition and Grant Services is conducting market research to identify sources capable of providing one large-area 2D X-ray flat panel detector for cone-beam CT and fluoroscopy imaging, with responses due May 12, 2026. No set-aside is anticipated at this stage; the small business set-aside determination will be made based on market research results.
The detector must support human-sized phantom development and testing with an active imaging area of at least 42.7 cm × 42.7 cm, pixel pitch not exceeding 170 μm, MTF of at least 50% at 1 lp/mm, and DQE of at least 70%. The unit must operate across 40–150 kVp energy ranges with frame rates of 25 fps (fluoroscopy), 30 fps (fluoro zoom if offered), 40 fps (CBCT projection), and 4 fps (radiography full resolution). Air cooling is required; operating temperature must span 19–49°C (or wider); and radiation tolerance must reach at least 2,000 Gy. Weight may not exceed 15 kg. Lag on the first frame must not exceed 3%.
Delivery shall include complete operational kit with all electronics, interfaces, cables, adapters, and documentation, plus minimum one-year warranty and one-year remote technical support. The FDA will accept brand-name or equivalent products meeting or exceeding all specifications. NAICS code is 334510 (Electromedical and Electrotherapeutic Apparatus Manufacturing) with a 1,000-employee size standard. Responses limited to 10 pages (excluding attachments and data sheets) in PDF or Word format should include company information, UEI/CAGE codes, SAM.gov registration, detailed technical capability statements with compliance matrices, delivery timelines, warranty terms, past performance references, and optional pricing. Submit to Freshta Javid at Freshta.javid@fda.hhs.gov by May 12, 2026 at 4:00 PM Eastern Time.
Notice text
Please refer to the attachments.
Attachments
| File | Type | Posted |
|---|---|---|
| Requirements Document.pdf | ||
| Sources Sought Notice.docx | DOCX document |
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