1. RECEIVE TEST
Elevation Diagnostics is now providing Covid-19 Testing Services for qualifying Businesses and Organizations
We provide full-service testing for our customers.
Here's how it works:
3. SEND TO LAB FOR PROCESSING
4. RECEIVE DIGITAL RESULT
Elevation Diagnostics Covid-19 Saliva Test Kit
Covid-19 Saliva Test
FDA EUA Authorized
As effective as Nasal Swab Testing
Tests for Active Infection of Sars-Cov-2
For Asymptomatic or symptomatic baseline testing
24-48hr results after shipping to lab
Why Saliva is better for Covid-19 Testing?
FDA EUA diagnostic test with 95% – 99% accuracy
Currently being used across the country for Covid-19 testing
Does not require nasal swab to be lodged deep into the nasal cavity
Allows for easy screening of large groups
Screen at home before returning to work
Fast turnaround time
No refrigeration required
Saliva is the easiest way to get tested!
Who is this test for:
This test is for organizations and businesses in need of non-invasive and reliable Covid-19 testing such as hospitals, clinics, nursing homes, universities, boarding schools, manufacturers and any high risk retail or business organizations. Elevation Diagnostics is able to help you assess your testing needs to provide comprehensive and easy baseline testing.
How is the test administered:
Tests are delivered and can be administered by either a healthcare professional or a trained HR professional. The OM-505 device allows for easy testing of large groups of individuals. Using the overnight shipping materials, the samples are delivered to a CLIA-certified lab with results digitally available in 24-48hrs after lab receipt. Results are available to both individuals and the representing organization and are easy to access via Elevation Diagnostic’s result portal.
*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. Learn more about the Emergency Use Authorization and Patient Fact Sheet