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Text Content

Solutions

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FROM TEST TO TREAT


ON/GO™ AND ON/GO ONE™ RAPID COVID-19 SELF-TESTS AND COMPANION APP


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OUR MISSION IS FREEDOM THROUGH KNOWLEDGE.

We believe everyone, everywhere should have the ability to live happier and
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ON/GO AND ON/GO ONE AT-HOME COVID TESTS


WHAT ARE ON/GO AND ON/GO ONE TESTS?

Whether you're looking for something to have on hand or for something that fits
in the palm of your hand, the On/Go and On/Go One rapid COVID-19 antigen
self-tests and companion app make testing quick, simple and portable. For those
at home and those on the go. On/Go and On/Go One are there for you!

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ON/GO FOR MY BUSINESS


GET BACK TO THE BUSINESS OF PEOPLE

At On/Go, we want to empower you to keep your employees safe, show them care and
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the best solution for keeping your work family safe.

Solutions for my Business




ON/GO FOR GOOD


ON/GO FOR GOOD- JOIN THE MOVEMENT

On/Go for Good is a charitable initiative within Intrivo that was created to
engage in philanthropy and support humanitarian causes across the world,
beginning with the crisis in Ukraine.
‍

Learn more & get involved!



THE ON/GO APP


BEFORE YOU TEST, INSTALL THE ON/GO APP

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DISCLAIMER

The On/Go and On/Go One tests have not been FDA cleared or approved but have
been authorized by FDA under an Emergency Use Authorization (EUA). These
products have been authorized only for the detection of proteins from
SARS-CoV-2, not for any other viruses or pathogens; the tests are 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.

The On/Go COVID-19 Antigen Self Test and the On/Go One COVID-19 Antigen Home
Tests are lateral flow chromatographic immunoassays intended for the qualitative
detection of the nucleocapsid protein antigen from SARS-CoV-2 in anterior nasal
swab specimens directly from individuals within 7 days of symptom onset or
without symptoms or other epidemiological reasons to suspect COVID-19

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