Our solution is the first all-in-one COVID-19 solution that combines our FDA authorized, best-in-class rapid self-tests with cutting-edge technology to help protect campers, counselors and staff.
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!
For in vitro diagnostic use only. Must be age 2+ to use these tests.
Learn more about On/Go One and On/Go.
Our top-rated iOS and Android mobile app delivers an intuitive testing experience. With over 30,000 five-star reviews, the On/Go app provides rapid test results, tracks your testing history and lets you easily share results with those who need to know.
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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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