3 COVID-19 Tests & Cue Reader
3 COVID-19 Tests & Cue Reader
3 COVID-19 Tests & Cue Reader
3 COVID-19 Tests & Cue Reader
3 COVID-19 Tests & Cue Reader

3 COVID-19 Tests & Cue Reader

4.8 stars with 16K+ ratings in App Store
At-Home test
Select quantity
$349
Cue+ Member Price$294.20

Cue's COVID-19 test is an FDA-authorized* at-home test to detect SARS-CoV-2, the virus that causes COVID-19. Cue’s test matched lab results with 97.8% accuracy in an independent study by Mayo Clinic. Results are delivered to your mobile smart device in 20 minutes.

If you test positive for COVID-19 with your Cue test, you can get Cue Care® through the Cue Health App at no additional cost, which includes a telehealth consult and same-day medication delivery, if prescribed (cost of medication not included).

• Results in 20 minutes
• Must be used with a Cue Reader (included)
• HSA/FSA eligible

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Trusted by 1.7 Million Users
FDA-approved
Tests
On Demand
Telehealth
FDA-approved Treatments

About
3 COVID-19 Tests & Cue Reader

Better care starts
with Cue

Timing is critical when it comes to knowing if you have COVID-19 so you don’t miss your treatment window or risk infecting others. With Cue, test anytime and get highly accurate results in 20 minutes.
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Lab-quality technology
Cue's COVID-19 test uses nucleic acid amplification testing (NAAT), which can detect even small amounts of virus with a nasal swab just like lab-quality tests, but without the need for a doctor's visit or the 24+ hour wait.
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Highly accurate
According to a Mayo Clinic study, Cue's COVID-19 test is 98% accurate and compares to PCR-quality laboratory tests. Unlike at-home antigen tests, Cue's results don’t require retesting, even if you're asymptomatic.
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Timing is critical
Did you know you may need to take three COVID-19 antigen tests over several days to get an accurate negative result ? In that time, you could be infecting others without knowing it. With Cue’s molecular test, you can trust your results the first time - keeping yourself and your loved ones safe.
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Compatible with future tests
The Cue Reader was designed by engineers and doctors to work with current and planned future Cue molecular tests across different health categories, including respiratory, sexual, and reproductive health.

How It Works
with Cue

Access fast, convenient care and discreet home delivery today. Get started in 4 easy steps.

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Insert your Cartridge into the Reader

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Use the Wand to collect a sample from the lower part of each nostril

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Insert the Wand into the Cartridge

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Receive results in 20 minutes via the Cue Health App

Cue customers say it best

It's amazing how easy and convenient Cue is to use. And getting highly accurate results in just 20 minutes is a game changer for me.

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Luis V.

Los Angeles, CA

I carry my Cue everywhere I travel. Its ability to get a near-instant, supervised digital test result on my phone has been a lifesaver to comply with the constantly changing location-specific testing requirements.

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Aaron W.

New York, NY

Since I discovered Cue COVID-19 tests, traveling has been way easier! Cue made my digital nomad life even better and more secure! I love how quick the results come in.

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Isabel Q.

San Francisco, CA

Carrying Cue in my bag while traveling has allowed me to get lab-quality results abroad and within 20 minutes, removing the hassle of finding testing sites compliant with the regulatory administrations internationally.

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Alberto P.

Chicago, IL

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Are you at risk for developing severe COVID-19?

Nearly 75% percent of US adults have risk factors for developing severe COVID-19.1 Answer a few short questions to find out if you have any of the risk factors.

*Cue COVID-19 Test for Home and Over The Counter (OTC) Use: The Cue COVID-19 Test for Home and Over The Counter (OTC) Use has not been FDA cleared or approved, but it has been authorized by the FDA under an Emergency Use Authorization (EUA). This product has been authorized only for the detection of nucleic acid from SARS-CoV-2, not for any other viruses or pathogens. 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. § 360bbb-3(b)(1), unless the declaration is terminated or authorization is revoked sooner.

Resources
¹ https://covid.cdc.gov/covid-data-tracker/#datatracker-home
² https://covid19.who.int/#:~:text=Globally%2C%20as%20of%204%3A24pm,vaccine%20doses%20have%20been%20administered.
 

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Download the Cue Health App to access shopping, test results, and treatment services. 

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4.8 stars with 16K+ ratings in App Store

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