Inito, homegrown startup clears US FDA regulatory pathway for Fertility Monitor. Inito becomes the first Indian home diagnostic device startup to achieve the milestone.
Inito, a Bengaluru-based medical technology startup, has cleared the regulatory pathway of the United States Food and Drug Administration (FDA) for its Fertility Monitor. By clearing this, Inito has become the first designed, engineered and manufactured in India home diagnostic device to achieve this milestone. This paves the way for the product’s launch in the US, and also allows access to countries that have signed the Mutual Recognition Agreement (MRA) with the FDA.
Smartphones to perform diagnostic tests at home.
Inito’s Fertility Monitor is a small device that enables smartphones to perform lab-grade fertility diagnostic tests at home. By measuring two fertility hormones in urine – Estrogen & Luteinizing Hormone (LH) – along with AI based data analytics in the App, Inito understands the cycle variations for every individual user, giving highly accurate results unique to every woman’s body.
The US FDA maintains strict regulatory control over all medical devices to ensure accuracy & safety for the end-user. Over the course of more than a year, Inito’s flagship device has been subjected to a series of clinical studies, manufacturing facility setup tests as per GMP standards, and company-wide Quality Management System, ensuring the reliability and efficacy of the device.
The clearance of the regulatory process of the Fertility Monitor for the US market comes at a particularly critical juncture due to the ongoing COVID-19 pandemic. The rapid spread of the disease has overwhelmed an already burdened healthcare system, with hospitals focused entirely on its treatment and containment.
As a result, many couples facing trouble conceiving have been left with nowhere to turn. This issue is especially pressing given the difficulty many couples face in getting pregnant, with 1 in every 3 couples taking over six months to conceive. Inito’s Fertility Monitor offers millions of aspiring parents a chance to overcome these difficulties without stepping out of their homes.
“Inito has always been committed to building a global home diagnostic testing company headquartered out of India, and this milestone takes us one step closer to that ambition. The coming years will see home diagnostics become an integral part of the medical ecosystem, and we’re proud to be among the leaders of this revolution,” said Aayush Rai, Co-Founder of Inito. “Clearing the FDA regulatory pathway speaks to the commitment and dedication of our team, who have upheld the highest standards of engineering, user experience, and clinical validation throughout the course of development,” he added.
About Inito:
Inito is India’s first Y Combinator backed medical device startup building the next generation of home diagnostic devices that are not just accurate and reliable, but are also smart and easy to use. Its proprietary technology allows a single device to do dozens of diagnostic tests at home. Based out of Bangalore, the company was started by IIT Roorkee alumnus, Aayush Rai and IIT Madras alum, Varun AV in 2015, to help people get healthier and happier while reducing the burden on the healthcare system & doctors.
Inito’s patented ‘Flat-lens’ technology allows dozens of diagnostic tests for fertility, diabetes, Vitamin D, Thyroid etc. and more on a single device connected to a smartphone. A study by IIT Delhi determined the device to achieve a 99.12 percent correlation with clinical-grade instrumentations which cost up to 100 times more and are 10 times bigger. As of now, the device supports fertility tests and other tests like Diabetes, Thyroid and Vitamin D tests are soon to be added to the device.
