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
PSC
6525 Imaging Equipment And Supplies: Medical, Dental, Veterinary
Place of performance
Silver Spring, Maryland 20993, United States
Points of contact

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

Files attached to this notice, newest first
File Type Posted
Requirements Document.pdf PDF
Sources Sought Notice.docx DOCX document

On GovTribe

Work this opportunity on GovTribe

  • Track it in your pipeline
  • Find teaming partners
  • Similar opportunities
  • Ask GovTribe AI about this opportunity