What is the distinctiveness of Cellex among several coronavirus antibody rapid diagnosis tests?

Cellex Covid-19 rapid diagnostic tests measure both IgM and IgG, so we can find out both whether we are currently infected (IgM) and whether we previously had the disease (IgG). Currently, there are many brands of antibody tests in the market, although the Turkish government has not permitted the sales and distribution of them yet. Many of these tests do not have confirmed qualifications. The difference of Cellex among several coronavirus antibody test manufacturers is that it has a deep-rooted experience of years in the production of rapid diagnostic tests. Cellex was the first company to get FDA approval in the United States after the spread of coronavirus infections all over the world. In the United States, FDA approval requirement applies to all medical products, tests and drugs as the most stringent and detailed government control in the world. Globally, the American FDA approval in health is considered the gold standard. In this respect, Cellex, which was the first brand to obtain FDA approval in the USA as of April 1, provides the most reliable results among various rapid diagnostic test kits. The sensitivity and specificity rates of the kit are 93.8% and 95.6% respectively.