• COVID-19 Testing Solutions, Made in America

COVID 19 Rapid Result Tests

Made in America

Dual-Line COVID-19 IgG/IgM Rapid Result Serology Tests

The Rapid Result COVID-19 Test Cassettes produce results in less than 15 minutes with just a small blood sample. Implemented correctly, the use of these test kits can allow for the thoughtful allocation of testing supplies where they are needed most. The FDA has issued emergency authority for the distribution of the Rapid Result Test Cassettes due to critical need of a more proactive solution.

  • Manufactured at SA Scientific Ltd.
  • Results in 15 minutes
  • Small sample sizes (fingerstick)
  • Sold in kits of 25
  • IgM may appear in blood within 3-5 days. IgG may appear as soon as 1-2 weeks.
  • Shelf life of up to 12 months from manufacture date
  • Tests should be administered by a licensed medical professional
  • Verification of use case will be required prior to shipping

We have a fact sheet for providers and test administrators (download here), as well a fact sheet for patients and employees, (download here).

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Antibody Tests are primarily intended for point of care application, they are not yet intended for home use without the oversight of a clinician to interpret the test results, record and report data pertinent to public health, and develop/discuss an appropriate care plan if necessary.

Negative results do not rule out SARS-CoV-2 infection, particularly in those who have been in contact with the virus. Regular testing is recommended. If acute infection is suspected, direct testing for SARS-CoV-2 is necessary.

Positive results may be due to past or present infection with non-SARS-CoV-2 coronavirus strains (coHKU1, NL63, OC43, or 229E). Consider follow up testing with molecular diagnostic to rule out infection in these individuals. To mitigate risk of false positive results, consider follow-up testing using a second, different rapid test, i.e., total antibody detection to dual line IgG/IgM assay, etc.

Results from one antibody test should not be used as the sole basis to diagnose or exclude SARS- CoV-2 infection or to inform infection status. Tests are intended for use as an aid in identifying individuals with an adaptive immune response to SARS-CoV-2, indicating recent or prior infection.

Additional information including clinical validation studies, fact sheets, and specific recommendations for asymptomatic testing programs available to healthcare providers upon request.

This test has not yet been reviewed by the FDA.

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