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  • COVID-19: Endemic Disease
  • Products
    • ASSURE-100 Home Tests
    • ASSURE-100 POC Tests
    • Buy ASSURE-100 Tests
  • News & Updates
  • Contact Us
  • BUY TESTS
January 2025 COVID-19 Forecast: Dominance of the XEC Variant and Public Health Strategies

January 2025 COVID-19 Forecast: Dominance of the XEC Variant and Public Health Strategies

by Oceanit | Jan 13, 2025 | Future, General

January 2025 COVID-19 Forecast: Dominance of the XEC Variant and Public Health Strategies As 2025 begins, the global health community continues to grapple with the ever-evolving SARS-CoV-2 virus. This January, the XEC variant has emerged as the dominant strain,...
COVID-19 Winter Wave: Holiday Season Surge in 2024–25

COVID-19 Winter Wave: Holiday Season Surge in 2024–25

by Oceanit | Jan 9, 2025 | Future, General

COVID-19 Winter Wave: Holiday Season Surge in 2024–25 As the holiday season unfolds, the United States faces a significant COVID-19 winter wave, with infection rates climbing across multiple regions. Seasonal factors, increased travel, and gatherings have contributed...
COVID-19 Burden Estimates for 2025: Illness, Hospitalizations, Deaths

COVID-19 Burden Estimates for 2025: Illness, Hospitalizations, Deaths

by Oceanit | Jan 9, 2025 | Future, General

COVID-19 Burden Estimates for 2025: Illness, Hospitalizations, Deaths As the United States enters the fifth year of managing the COVID-19 pandemic, preliminary estimates for 2025 provide critical insights into the virus’s impact. These projections, based on data from...

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Copyright 2025 Oceanit Foundry LLC. The ASSURE-100 Rapid COVID-19 Test has not been FDA cleared or approved, but has been authorized by FDA under an EUA. This product has been authorized only for the detection of proteins 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.
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