Get Tested for COVID-19 Without Leaving Your Home

FDA Authorized

COVID-19 Test – Only $109

Type: Saliva

Painless

Self-Administered Test

Results Within 24-48 Hours

The Gold Standard In COVID-19 Testing

Why is this item marked as FSA Eligible?

This item is marked as FSA eligible to identify that it MAY be purchased using a flexible spending account (FSA):

FSA Eligible Item

What is a Flexible Spending Account (FSA)?

A FSA (Flexible Spending Account) allows use of the funds an individual has designated to be set aside pre-tax for medical expenses, typically with their employer, when selecting healthcare programs during the previous year.

What types of purchases are FSA eligible?

Over-the-counter medical supplies and equipment are considered reimbursable by an FSA account in 2020 and include the following categories:

  • Contact lens solution
  • Prescription contact lenses with correction only
  • Diagnostic devices (i.e. blood pressure and blood glucose monitors)
  • Durable medical equipment and goods
  • Insulin
  • Prescription medications

Note: Although the IRS sets guidelines for FSA programs, individual employers have the final determination of which expense are covered by their FSA programs.

HOW IT WORKS

Register Your Kit Online

Spit in Collection Tube

Mail Test (free shipping)

Get Your Results via Text

BEFORE ORDERING

In the past two weeks, what has been your exposure to COVID-19?

Close contact is spending a prolonged period of time within 6 feet of someone or was exposed to a cough or sneeze.

  • I may have had close contact with someone who has been diagnosed with or presumed to have COVID-19
  • I may have had close contact with someone who is sick but has not been diagnosed with COVID-19
  • I live or work in a congregate setting where people reside, meet, or gather in close proximity such as a healthcare setting, office building, homeless shelter, assisted living facility, group home, prison, detention center, school, or workplace

This test has been authorized by the Food and Drug administration under the Emergency Use Authorization. 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.