COVID-19 Saliva Test Kit
At-Home Testing for Coronavirus
Shipping included with price.
The First FDA Emergency Use Authorized at-home COVID-19 Saliva test.
COVID-19 At-Home Saliva Test Kit $144
How the COVID-19 Saliva Test Works
Order Your Kit
Once received via express mail you must register your kit at
After registering your kit, carefully follow the onscreen instructions and proceed to collect your saliva in the provided tube.
Results will be made available within 72 hours of the lab receiving your sample. Please view your results immediately and follow the recommendations given.
In the Press
How Much Does a
COVID-19 Home Test Kit Cost?
Our COVID-19 test kit costs $144 out-of-pocket, and HSA and FSA cards are accepted as payments. You may be eligible for further insurance coverage if prescribed by a doctor. However, please note we will not file claims with insurance companies. As money is disbursed from the federal government, it is possible that the cost of the home saliva test kit may be fully covered in the future. We will be monitoring any changes closely and update our customers accordingly. If you are a health care provider, you may qualify for different pricing.
Who Should Get Tested for Coronavirus?
Tests will only be given out based upon likelihood of infection per CDC guidelines and national testing capacity. However, if you are not qualified for a test at first, you may be once testing capacity increases and we will alert you automatically when tests become available to people at your risk level.
If you have further questions about your eligibility for COVID-19 testing, we recommend reaching out to your primary healthcare provider to see if testing is right for you at this time. If you are experiencing severe or life-threatening symptoms, please seek immediate medical care from a healthcare professional or call 9-1-1.
How to Get the First
COVID-19 Testing Kit
Our self-collected coronavirus testing kit uses a hassle-free saliva sample to determine if you are infected with the SARS-CoV-2 virus. We’ve partnered with labs operating under the Emergency Use Authorization guidelines issued by the FDA. Our COVID-19 home saliva test kits ship with the highest priority postage for the fast delivery to your home and back to the lab. Within 72 hours of the lab receiving your sample, you will receive secure digital results.
After you receive your results, you will have an opportunity to have a telehealth consult with an independent licensed physician or other healthcare provider, who can answer any questions you may have about your test results and help determine next steps.
Your Test Results
Secure Digital Results
All of Vitagene’s laboratory partners that are conducting COVID-19 testing have had their validation data and reports reviewed by the FDA under the Emergency Use Authorization framework.
What Happens Next
You will receive your COVID-19 test results at home within 72 hours of the lab receiving your saliva sample. Your test results will confirm whether or not you are infected with SARS-CoV-2, the strain of coronavirus responsible for COVID-19.
Select the profile that best suits you
Vitagene tests are evaluated and approved (if appropriate) by an independent board-certified physician in your state.
Our partner lab RUCDR Infinite Biologics is CLIA-certified (Clinical Laboratory Improvement Amendments). This means they have to meet high standards to obtain both state and federal certifications and submit themselves to regular inspections.
Non-invasive Collection Method
We use a simple and effective saliva collection method. This method enables you to collect your own sample and is more comfortable than other methods such as nasal swabs.
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This test has been authorized by the FDA under an Emergency Use Authorization for use by authorized laboratories. This test has not been FDA cleared or approved. This test has been authorized only for the detection of nucleic acid from SARS-CoV-2, not for any other viruses or pathogens. This test is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostic tests for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Act, 21 U.S.C. § 360bbb-3(b)(1), unless the authorization is terminated or revoked sooner. For more information, please refer to the patient and healthcare provider fact sheets.