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MAXIM BIOMEDICAL, INC

UEI: YV7LJS28ERK8CAGE: 4EJW3

MAXIM BIOMEDICAL, INC is a federal contractor, registered under UEI YV7LJS28ERK8 and CAGE code 4EJW3. It has been awarded $128,723,256 in federal contracts. Primary work spans In-Vitro Diagnostic Substance Manufacturing, Unknown NAICS, and Medical Laboratories. Top awarding agencies include Department Of Health And Human Services, Department Of Defense, and Department Of Health And Human Services (hhs).

Contact Information

Registration and classification details

Registration

UEI Code

YV7LJS28ERK8

CAGE Code

4EJW3

Entity Structure

Corporate Entity (Not Tax Exempt)

Established

N/A

Business Classifications

For Profit OrganizationAsian-Pacific American OwnedManufacturer of Goods

NAICS Codes

325413In-Vitro Diagnostic Substance Manufacturing(Primary)
325414Biological Product (except Diagnostic) Manufacturing
334516Analytical Laboratory Instrument Manufacturing
334519Other Measuring and Controlling Device Manufacturing

Federal Contracting Overview

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

AI Capability Profile

MAXIM BIOMEDICAL, INC specializes in the manufacturing of in-vitro diagnostic substances and operates within the medical laboratory services domain, delivering critical public health solutions under federal contracts. The company’s core capabilities center on the development, production, and regulat...

MAXIM BIOMEDICAL, INC specializes in the manufacturing of in-vitro diagnostic substances and operates within the medical laboratory services domain, delivering critical public health solutions under federal contracts. The company’s core capabilities center on the development, production, and regulatory-compliant scaling of diagnostic test kits, including over-the-counter COVID-19 antigen tests, demonstrating expertise in molecular and immunoassay-based diagnostic platforms. Their technical proficiency spans GMP-compliant manufacturing processes, quality control for clinical-grade reagents, and the integration of diagnostic systems into public health response frameworks. A key differentiator is their ability to rapidly transition diagnostic products from development to large-scale deployment under urgent public health exigencies, aligning with FDA emergency use authorization pathways and CDC testing protocols. The contractor has established a consistent relationship with the Department of Health and Human Services, supporting both diagnostic manufacturing and laboratory operational integrity through contract modifications and closure activities. Their work with HHS reflects deep familiarity with federal health emergency response mechanisms, regulatory documentation, and the lifecycle management of diagnostic supply chains. Industry focus is narrowly defined by NAICS 325413 for in-vitro diagnostic substance manufacturing and 621511 for medical laboratory services, positioning MAXIM BIOMEDICAL as a niche provider in the public health diagnostics sector. They serve the intersection of clinical diagnostics and federal preparedness, with specialization in point-of-care and self-administered testing systems. As a small business structured as a 2L entity based in Rockville, Maryland, MAXIM BIOMEDICAL operates within the federal biomedical supply chain without formal government certifications. Their geographic proximity to federal health agencies and regulatory bodies enhances responsiveness and compliance coordination in the U.S. government market.

Key Performance Metrics

Awards Count

30

All time

Active

1

Currently performing

Completed

29

Past period of performance

Total Awards

All time

Contracts

Prime · all time

Subcontracts

Sub · all time

Grants

Prime · all time

Subgrants

Sub · all time

Award Analytics & Distribution

Awards by Agency
Awards by NAICS
Export
325413 - In-Vitro Diagnostic Substance Manufacturing$107.3M83.4%
- Unknown NAICS$15.5M12%
621511 - Medical Laboratories$5.3M4.1%
Others - Other NAICS codes (3 codes, <0.5% each)$689.6K0.5%
Awards by Agency Over Time
Awards by Place of Performance

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NAICS: 621511
New
SLED
Statewide Sample Collection, Drug Screen & Confirmatory Testing
Solicitation # J28030
The Department of Judiciary for the State of Hawaii is soliciting bids under solicitation J28030 for statewide sample collection, initial drug screening, and confirmation testing. The contractor is responsible for collecting urine specimens from individuals referred by the First, Second, Third, and Fifth Circuit courts at their own or an approved subcontractor's facilities. Initial screenings must utilize the EMIT system or an approved equivalent, while confirmation testing must be performed using gas chromatography/mass spectrometry by a company licensed and accredited in Hawaii. The contractor must provide these services seven days a week and submit written procedures to the Officer-in-Charge to ensure samples are not tampered with during collection. The contract is for an initial twenty-four month term from July 1, 2027, through June 30, 2029, with the possibility of two additional twelve-month extensions. Award will be granted to the lowest responsive and responsible bidder, with preferences considered for Hawaii-based products and other statutory categories. Payment is based on the actual number of samples collected per month at the unit bid cost, with invoices submitted separately for each circuit. The contractor must maintain compliance with various Hawaii state laws, including tax clearances, unemployment insurance, and prepaid health care requirements.
Department of Judiciary

POSTED

about 17 hours ago

DEADLINE

in 25 days
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NAICS: 325413
New
DIBBS
CULTURE MEDIUM, THAYER-
Solicitation # SPE2DS-27-T-1066
Solicitation SPE2DS-27-T-1066 is a request for quotations issued by the DLA Troop Support Medical Supply Chain for the procurement of one package of Thayer-Martin Modified (MTM II) Agar culture medium, identified by NSN 6550-01-711-1542. This dark brown, ready-to-use plated medium is specifically designed for the isolation of pathogenic Neisseria from specimens containing mixed flora of bacteria and fungi. The product is delivered in packages of 100 plates and requires strict refrigeration storage between 2 to 8 degrees Celsius (36 to 46 degrees Fahrenheit) and must not be frozen. The contract mandates a non-extendable shelf life of three months, with a requirement that no more than 14 days elapse between the date of manufacture and the date of delivery to the government. Delivery is set for JBER, Alaska, with a required delivery date of October 27, 2026, under FOB Destination terms. Packaging must be commercial and sealed to prevent damage, with marking adhering to Medical Marking Standard No. 1 and shelf-life labels following MMS1C. Administrative requirements include electronic invoicing via the Wide Area WorkFlow system and compliance with various FAR and DFARS clauses, including the Buy American Act, Berry Amendment, and safeguarding of covered defense information. Evaluation will consider technical data for any alternate products offered and may include HUBZone price evaluation preferences. Inspection and acceptance will occur at the destination.
MEDICAL SUPPLY CHAIN MD SURG FSF

POSTED

about 22 hours ago

DEADLINE

in 5 days
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NAICS: 541330
New
Federal
AIR FORCE CRYPTOLOGIC OFFICE COMMERCIAL SOLUTIONS OPENING
Solicitation # FA7037-21-S-C001
The Air Force Cryptologic Office (AFCO) Cyberspace Intelligence Surveillance and Reconnaissance and Multi-Domain Innovation Division is soliciting innovative commercial capabilities through Commercial Solutions Opening FA7037-21-S-C001. The agency is seeking mature technologies and innovative services in Electromagnetic Warfare, Information Operations, and electromagnetic digital communications, with a specific goal of achieving a field demonstration within one year. The procurement process is divided into two phases: Phase I requires the submission of a quad chart and a white paper, while Phase II consists of full proposals by invitation only. Awards may be issued as traditional contracts or Other Transactions (OT), with potential funding ranging from 50,000 dollars to 50 million dollars over a period of performance lasting between one and five years. The evaluation process is based on technical merit, importance to agency programs, and fund availability, utilizing peer or scientific review to select offerors. Successful projects are expected to follow a structure of base period tasks to demonstrate feasibility, followed by option tasks for design, fabrication, testing, and evaluation. Because the work supports DoD ISR-Cyber capabilities, offerors must possess the necessary personnel and facility security clearances to handle classified work independently. All acquired technologies are treated as commercial items under 10 USC 3458 and DFARS 212.70. Submissions are managed by Carissa Heuertz, and the performance location is identified as San Antonio, Texas.
Department Of Defense

POSTED

1 day ago

DEADLINE

in 11 months
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NAICS: 621511
New
International
In-Vitro Diagnostics, Point of Care Testing & Pathology Services Project_1717
Solicitation # Project_1717
Supply Chain Coordination Limited, acting for NHS Supply Chain, is establishing an open national framework agreement for the provision of In-Vitro Diagnostic Devices, Point of Care Testing Products, and Related Pathology Services. The scope of the procurement is extensive, covering pathology managed services, reagent rental agreements, pathology software, and core laboratory equipment and consumables across multiple disciplines, including biochemistry, microbiology, immunology, cellular pathology, virology, haematology, genomics, molecular testing, and reproductive sciences. Additionally, the framework includes point of care testing and specimen collection and storage. The procurement is organized into three distinct lots: Pathology Managed Services, Pathology Software Solutions, and Diagnostics Testing Solutions. The estimated total value for the initial period is 703,101,796 GBP excluding VAT, with a potential total value of approximately 2,545,824,000 GBP excluding VAT over the full eight-year framework duration. The estimated contract period runs from October 18, 2027, to October 17, 2029, with an overall framework end date of October 17, 2035. Proposals must be submitted electronically by December 16, 2026. Evaluation for Lots 1 and 2 is weighted at 80 percent for non-financial quality, 10 percent for social value, and 10 percent for price. Lot 3 is evaluated based on 60 percent non-financial quality, 30 percent cost, and 10 percent social value.
Supply Chain Coordination Limited

POSTED

1 day ago

DEADLINE

in about 2 months
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