Quickfinder COVID-19 Antigen Home Tests - MAde in USA

FDA - authorized self test
Results in 15 min
Made in USA
Easy to use - best results

Buy online or in your preferred Pharmacy

Quickfinder Antigen Home Test is available at many pharmacies and online marketplaces. We manufacture our tests in Jackson - Ohio and are proud to offer a Made in US product. By manufacturing nationally, we can ensure short distances from the factory to the user. Stringent controls ensure excellent quality throughout. Quickfinder Antigen Home Test is the first choice for the safety of the whole family.

Our premises and warehouses in Jackson, Ohio, allows us to deliver products effortlessly and quickly all over USA and beyond.

Are you under 
a healthcare plan?


If you have health insurance through an employer, the Marketplace, Medicare, or Medicaid, your insurance will pay for 8 at-⁠home tests each month for each person on your plan. freecovidtest.us.com made it easy just join our service an we take care of the rest.
Got COVID-19 or Flu? 

Make sure how to protect you and your family. Only 15 minutes and 4 steps to rest assured. 

Quickfinder Antgen home test For the ones you love

Always safety first


Why Quickfinder Antigen Home Test?

Quickfinder COvid 19 antigen home test

FDA-EUA Emergency Use Authorization Made in USA Efficient supply  Qualifies for Federal, State and Health Insurance procurement requirements and preferences

Eligible under public health emergency

If you have health insurance through an employer, the Marketplace, Medicare, or Medicaid, your insurance will pay for 8 at-⁠home tests each month for each person on your plan.

Easy to use

Easy-to-Use Nasal Swab Test, Quickfinder COVID-19 Antigen Rapid Test is the simplest way to detect SARS-CoV-2 nucleocapsid protein antigen. It only takes 4 steps and 15 minutes  

Reliable and safe

 Quickfinder  COVID-19 Antigen Rapid Test, helps you better care for yourself and protects your friends, family, and community members from potential exposure. Easy-to-Understand Results.

In the USA, this product has not been FDA cleared or approved; but has been authorized by FDA under an EUA;
This product has been authorized only for the detection of proteins from SARS- CoV-2, not for any other viruses or pathogens; and,
The emergency use of this product is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug and Cosmetic Act, 21 U.S.C. § 360bbb3(b)(1), unless the declaration is terminated or authorization is revoked sooner.
For more information on EUAs please visit:https://www.fda.gov/emergency-preparedness-and-response/mcm-legal-regulatory-and-policy-framework/emergency-use-authorization
For the most up to date information on COVID-19, please visit: www.cdc.gov/COVID19

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