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VERACYTE INC.

Parent1 subsidiaryUEI: JS7GBP6LCMN6CAGE: 60GJ7

VERACYTE INC. is a federal contractor, registered under UEI JS7GBP6LCMN6 and CAGE code 60GJ7. It has been awarded $6,798,518 across 153 federal contracts. Primary work spans Medical Laboratories, In-Vitro Diagnostic Substance Manufacturing, and Surgical and Medical Instrument Manufacturing. Top awarding agencies include Department Of Veterans Affairs, Department Of Defense, and Department Of Health And Human Services.

Contact Information

Registration and classification details

Registration

UEI Code

JS7GBP6LCMN6

CAGE Code

60GJ7

Federal Contracting Overview

Award totals, agency breakdown, NAICS distribution, and geographic footprint.

AI Capability Profile

Veracyte, Inc. specializes in advanced molecular diagnostic services and reference laboratory solutions, primarily delivering genomic testing and precision diagnostics for clinical decision support. Their core capabilities include the deployment of next-generation sequencing platforms, such as the A...

Veracyte, Inc. specializes in advanced molecular diagnostic services and reference laboratory solutions, primarily delivering genomic testing and precision diagnostics for clinical decision support. Their core capabilities include the deployment of next-generation sequencing platforms, such as the Afirma Genomic Sequencing Classifier, and targeted molecular assays for thyroid and other endocrine disorders. The company provides high-complexity clinical laboratory services with a focus on diagnostic accuracy, algorithm-driven classification, and scalable reference lab infrastructure tailored to large-scale healthcare systems. Their technical expertise lies in genomic data interpretation, liquid biopsy analysis, and FDA-cleared diagnostic tools that reduce unnecessary surgeries and improve patient outcomes in oncology and endocrinology. Veracyte maintains a strong, sustained relationship with the Department of Veterans Affairs, consistently supporting VA medical centers through reference laboratory services and task-order-based genomic testing programs. Their work for the VA centers on delivering specialized diagnostic solutions across VISN networks, enabling standardized, high-quality testing for veterans in remote and urban facilities alike. The Department of Defense is also represented in their contract history, indicating capacity to meet federal defense healthcare requirements for advanced diagnostics. The company’s primary industry focus is medical laboratories under NAICS 621511, where they operate as a niche provider of genomic and molecular diagnostics within government healthcare delivery systems. They are positioned at the intersection of precision medicine and public health infrastructure, serving as a trusted partner for complex, evidence-based testing that informs clinical pathways. Veracyte, Inc. is a limited liability entity headquartered in South San Francisco, California, with a dedicated laboratory and research infrastructure supporting federal contract obligations. While no formal government certifications are listed, their operational model reflects adherence to CLIA, CAP, and HIPAA standards required for federal clinical lab services. Their geographic presence and technical specialization make them a key provider for federal agencies requiring advanced diagnostic capabilities.

Key Performance Metrics

Awards Count

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Total Awards

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Award Analytics & Distribution

Awards by Agency
Department Of Veterans Affairs$5.8M85.8%
Department Of Defense$694.9K10.2%
Department Of Health And Human Services$262.8K3.9%
Other agencies (1 agencies, <0.5% each)$6.4K0.1%
Awards by NAICS
621511 - Medical Laboratories$6.6M97.5%
325413 - In-Vitro Diagnostic Substance Manufacturing$116.0K1.7%
339112 - Surgical and Medical Instrument Manufacturing$44.1K0.7%
Others - Other NAICS codes (3 codes, <0.5% each)$10.5K0.2%
Awards by Agency Over Time
Awards by Place of Performance

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NAICS: 339112
New
Federal
SPS Sterilizer
Solicitation # 36C24526Q0758
Solicitation 36C24526Q0758 is a Firm-Fixed Price purchase order for the procurement and installation of five new steam sterilizers and five switch-over control systems for the Sterile Processing Service at the Baltimore VA Medical Center. The project includes the de-installation and disposal of existing equipment, facility work such as plumbing relocation and flooring leveling, and system validation performed by an OEM-trained representative. To ensure continuous operations, installation must be completed in two phases, with the first two units installed followed by the remaining three. While Belimed is the brand name of reference, the government will accept fully equivalent systems that meet specific dimensions and a minimum chamber volume of 275 liters. The award will be granted to the responsible quoter determined to be most advantageous based on technical capability, price, and past performance. Mandatory submission requirements include a detailed line-item worksheet, manufacturer authorization letters for distributors, and specific certifications regarding Service Contract Labor Standards. Delivery must be FOB Destination and completed within 12 months of the award. Contractors are required to maintain general liability insurance of 500,000 dollars per occurrence and comply with strict security prohibitions regarding covered telecommunications equipment. Invoices are to be submitted electronically in arrears upon the receiving and acceptance of goods and services.
245-NETWORK Contract Office 5 (36C245)

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NAICS: 339112
New
Federal
Automated Endoscope Reprocessor (BAMC, San Antonio, Texas)
Solicitation # HT940826QE040
Solicitation HT940826QE040 is a combined synopsis and request for quote issued by the Defense Health Agency for the procurement and installation of five automated endoscope reprocessors (AERs) at Brooke Army Medical Center in San Antonio, Texas. The scope of work includes the installation of units across the Gastroenterology, Pulmonary, and Pediatrics departments, as well as the deinstallation and hauling away of twelve existing Olympus OER Pro/Elite systems. The required AERs must be FDA Class II Medical Devices with 510(k) premarket notification, featuring dual-basin designs with cycle times of approximately 22 minutes and compliance with AS/NI/AAMI ST91 and CDC infection prevention guidelines. The contract also requires the provision of compatible hookup blocks, water filtration assemblies, vapor management accessories, a one-year commercial warranty, and comprehensive on-site clinical training for staff. This is a firm-fixed-price acquisition that is not set aside for small business concerns, though it allows for HUBZone price evaluation preferences. Award will be based on the most advantageous offer, considering price, technical literature demonstrating compliance with specifications, and the delivery and installation timeframe. All items must be delivered by November 15, 2026, and must adhere to DoD item unique identification and marking standards per MIL-STD-130 and MIL-STD-129. Quotes must be submitted electronically to the designated points of contact by September 16, 2026. Payment will be processed electronically through the Wide Area WorkFlow (WAWF) system.
Defense Health Agency

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