Presolicitation Notice – Z-SPEC Z-max X-Ray Fluorescence (XRF) Instrument

Closed Pre-Solicitation Posted

Solicitation number
NOI-FDA-133864
Agency
Responses due
Set-aside
No set-aside

Opportunity facts

Place of performance
Irvine, California 92612, United States

Notice details come from SAM.gov. Updated .

About this opportunity

The FDA Office of Acquisition and Grant Services intends to procure a Z-SPEC Z-max X-Ray Fluorescence instrument under a single-source justification, with capability statements due July 14, 2026. The procurement is restricted to Z-SPEC, Inc. (CAGE Code 21BJ9, East Greenbush, New York) as the sole manufacturer offering the proprietary Doubly Curved Crystal optical technology required to meet analytical specifications.

The instrument must achieve limits of detection of 0.03 ppm for elemental lead and 0.05 ppm for elemental mercury, accommodate sample masses from 0.05 to 3.0 grams, support calibration ranges from limit of detection to 10,000 ppm, and fit within a 30" W × 30" D × 30" H footprint with standard 110–120V power requirements. Place of performance is the FDA Irvine Medical Products Laboratory. The vendor must provide installation by a certified field service engineer, operator-level training for two users at delivery, and a minimum 12-month warranty covering parts, labor, and travel costs for OEM-trained service engineers.

The contract will be awarded on a Firm-Fixed-Price basis using simplified acquisition procedures for a value above $25,000 but at or below the Simplified Acquisition Threshold. Solicitation issuance is anticipated for July 21, 2026, with award expected on or before August 10, 2026.

Notice text

Refer to the attached NOI.

Files

File Type Posted
PreSolicitation_Notice_NOI-FDA-133864.docx DOCX document

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