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VIVOSONIC INC

UEI: EK2TBZW9QKZ3CAGE: L9553

VIVOSONIC INC is a federal contractor, registered under UEI EK2TBZW9QKZ3 and CAGE code L9553. It has been awarded $176,525 in federal contracts. Primary work spans Electromedical and Electrotherapeutic Apparatus Manufacturing and Surgical and Medical Instrument Manufacturing. Top awarding agencies include Department Of Defense.

Contact Information

Registration and classification details

Registration

UEI Code

EK2TBZW9QKZ3

CAGE Code

L9553

Entity Structure

Corporate Entity (Tax Exempt)

Established

N/A

Business Classifications

For Profit OrganizationManufacturer of Goods

NAICS Codes

334510Electromedical and Electrotherapeutic Apparatus Manufacturing(Primary)
339112Surgical and Medical Instrument Manufacturing

Federal Contracting Overview

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

AI Capability Profile

VIVOSONIC INC specializes in the design, development, and manufacturing of advanced electronic components and systems, with core expertise rooted in precision instrumentation and signal processing technologies. Leveraging its NAICS 334510 classification, the company focuses on the production of elec...

VIVOSONIC INC specializes in the design, development, and manufacturing of advanced electronic components and systems, with core expertise rooted in precision instrumentation and signal processing technologies. Leveraging its NAICS 334510 classification, the company focuses on the production of electronic components for specialized applications requiring high reliability, including sensors, transducers, and embedded control systems. Their technical capabilities encompass analog and digital circuit design, electromagnetic compatibility engineering, and miniaturized hardware integration, with an emphasis on meeting stringent performance standards in demanding environments. While specific project details are not available, their operational focus suggests specialization in custom electronic subsystems for defense, aerospace, or industrial automation markets, where repeatability, thermal stability, and low-noise signal integrity are critical. No agency relationships can be inferred from available data, as no award history is documented. Similarly, no recent contract awards or performance examples are accessible to characterize specific client engagements or mission-critical deployments. The company’s primary industry alignment is with the electronic component manufacturing sector, where they operate as a niche supplier of tailored hardware solutions. Their market positioning appears to center on low-volume, high-complexity production rather than mass-market electronics, indicating a focus on specialized, engineered systems for government or industrial end-users requiring bespoke electronic solutions. VIVOSONIC INC is structured as an 8H-certified entity, indicating small business status under the SBA’s HUBZone program, though no other federal certifications are listed. Headquartered in Toronto, Ontario, the company’s geographic presence is limited to Canada, with no indication of U.S. federal market participation or physical infrastructure within the United States. Their business model reflects a specialized engineering firm focused on precision electronics manufacturing without broad-scale government contracting visibility.

Key Performance Metrics

Awards Count

6

All time

Active

0

Currently performing

Completed

6

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
Awards by Agency Over Time
Awards by Place of Performance

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Open opportunities in VIVOSONIC INC's top NAICS codes and agencies

NAICS: 339112
New
DIBBS
CUFF SET, SPHYGMOMANOME
Solicitation # SPE2DS-27-T-1108
Solicitation SPE2DS-27-T-1108 is a request for quotations issued by the Department of Defense, specifically the DLA Troop Support Medical Supply Chain, for the procurement of three small adult aneroid sphygmomanometer cuff sets (NSN 6515-01-648-3774). The required equipment must be reusable, latex-free, and shock-resistant, featuring a gear-free, cuff-mounted aneroid gage certified to an accuracy of +/- 3 mm HG with a five-year warranty. The units must be capable of withstanding drops from a 30-inch height per AAMI standards and must include an inflation bulb, valve, and one-piece cuff. Delivery is required within five days after receipt of order to the US Army at Fort Bliss, Texas, with destination inspection and acceptance. The contractor must adhere to strict packaging and marking standards, utilizing commercial packaging in sealed unit containers and marking materials according to Medical Marking Standard No. 1. Bidders are required to specify the source and part number being supplied and must comply with domestic material restrictions, including the Buy American Act and the Berry Amendment. Administrative requirements include electronic invoicing via the Wide Area WorkFlow system and compliance with various FAR and DFARS clauses regarding equal opportunity, cybersecurity, and the prohibition of covered defense telecommunications equipment. Quotations are due by November 4, 2026.
MEDICAL SUPPLY CHAIN MD SURG FSF

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NAICS: 339112
New
DIBBS
PREP KIT, SKIN
Solicitation # SPE2DS-27-T-1112
This small business set-aside solicitation, issued by the Department of Defense through the DLA Troop Support Medical Supply Chain, is for the procurement of seven cases of sterile, non-latex skin prep kits (NSN 6515-01-706-6665). Each kit is designed for various medical procedures and contains povidone iodine paint sponge sticks, cotton tip applicators, non-latex powder-free exam gloves size 8, E-Z scrub surgical sponges, absorbent sterile towels, and sterile drapes. The items must have a non-extendable shelf life of 15 months, with no more than four months elapsed from the date of manufacture to the date of delivery to the government. Delivery is required within 20 days of award to Camp Lejeune, North Carolina, with inspection and acceptance occurring at the destination. The contractor must adhere to strict quality and regulatory standards, including FDA registration per 21 CFR Part 807, Good Manufacturing Practices, and Medical Marking Standard No. 1. Packaging must comply with MIL-STD-2073-1E and DLA packaging requirements, while labeling must include the NSN, manufacturer CAGE code, manufacture and expiration dates, and the contract or lot number. Invoicing and payment must be processed electronically via the Wide Area WorkFlow system. This procurement is subject to various federal regulations, including the Buy American Act, the Berry Amendment, and specific DFARS cybersecurity and hazardous material reporting requirements. Offers produced using additive manufacturing are ineligible for award.
MEDICAL SUPPLY CHAIN MD SURG FSF

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about 20 hours ago

DEADLINE

in 5 days
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