X-Ray Fluorescence (XRF) Instrument Irvine Medical Products Laboratory (IRVLMP)
SOL #: OC-2026-133864Sources Sought
Overview
Buyer
Health And Human Services
Food And Drug Administration
FDA OFFICE OF ACQ GRANT SVCS
Rockville, MD, 20852, United States
Place of Performance
Silver Spring, MD
NAICS
Analytical Laboratory Instrument Manufacturing (334516)
PSC
Chemical Analysis Instruments (6630)
Set Aside
No set aside specified
Original Source
Timeline
1
Posted
May 15, 2026
2
Response Deadline
May 21, 2026, 6:00 PM
Qualification Details
Fit reasons
- NAICS alignment with historical contract wins in similar service areas.
- Scope strongly matches core technical capabilities and delivery model.
Risks
- Past performance thresholds may require one additional teaming partner.
- Potential clarification needed on staffing minimums before bid/no-bid.
Next steps
Validate eligibility requirements, assign capture owner, and schedule partner outreach to confirm teaming strategy before submission planning.
Quick Summary
The U.S. Food and Drug Administration (FDA), specifically the Irvine Medical Products Laboratory (IRVLMP), is conducting market research through a Sources Sought / Request for Information (RFI) to identify potential sources for an X-Ray Fluorescence (XRF) Instrument. This instrument is required for elemental analysis of regulated commodities, focusing on the rapid, non-destructive detection of toxic heavy metals. Responses are due Thursday, May 21, 2026, at 2:00 PM Eastern Time.
Requirement Details
The FDA requires one (1) benchtop XRF Instrument with specific salient characteristics:
- Optics: Doubly Curved Crystal (DCC) x-ray optics with monochromatic excitation.
- Detection Limits: Limit of Detection (LOD) for elemental lead ≤ 0.03 ppm; LOD for elemental mercury ≤ 0.05 ppm.
- Sample Range: Sample mass range from 0.05 grams to 3.0 grams.
- Calibration: Calibration range from LOD up to ≥ 10,000 ppm.
- Configuration: Benchtop or portable, with a maximum footprint of 30" W × 30" D × 30" H.
- Power: 110–120V.
Contract & Timeline
- Type: Sources Sought / Market Research (not a solicitation)
- Set-Aside: None specified
- Response Due: May 21, 2026, 2:00 PM ET
- Published: May 15, 2026
- Place of Performance: Silver Spring, MD
Requested Information from Vendors
Interested vendors should provide:
- Company contact information, business size, and socioeconomic status.
- Applicable NAICS codes and associated business size.
- Manufacturer, product name, and model number of the proposed instrument.
- Detailed specifications demonstrating compliance with all salient characteristics.
- Country of manufacture.
- GSA Federal Supply Schedule (FSS) contract number, if applicable.
- Estimated delivery time and price range (for planning purposes).
Response Instructions
- Submission: Electronically via email to freshta.javid@fda.hhs.gov.
- Subject Line: "Sources Sought/RFI – OC-2026-133864 – XRF Instrument".
- Page Limit: Maximum ten (10) pages.
- Note: No debriefs or feedback will be provided. This RFI is for market research only and does not guarantee a future solicitation or commitment to award. The government will not pay for response costs.
People
Points of Contact
Freshta JavidPRIMARY
Files
Files
Versions
Version 1Viewing
Sources Sought
Posted: May 15, 2026