FDA Greenlights Second Model in Kronos Advanced Technologies Inc.'s Revolutionary Air Purifiers Line

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Kronos Advanced Technologies Inc.
Kronos Advanced Technologies Inc.

New FDA 510(k) Clearance for Model 8 Enhances Kronos' Medical-Grade Air Purification Offerings, Expanding Deployment in Healthcare and Commercial Sectors

Los Angeles, CA , July 10, 2024 (GLOBE NEWSWIRE) -- Los Angeles,CA  July 2024 (GLOBE NEWSWIRE) -- KRONOS ADVANCED TECHNOLOGIES, INC. (OTC MARKETS: KNOS) ("KNOS" or the "Company"), an innovation-driven product development company and creator of the patented Kronos® CORE air disinfection technology inside its advanced smart air purification devices, announced today that the U.S. Food and Drug Administration (FDA) has recently granted an additional 510(k) clearance to a flagship product, Kronos® Model 8, classifying it as a Class II Medical Device. This second FDA clearance was provided after a detailed review of the patented Model 5 device back in 2023, which utilizes patented High Voltage Field air disinfection technology proven to eliminate 99.9% of harmful airborne particles, including allergens, bacteria, fungi, and viruses, like COVID-19. This FDA clearance means our air purifiers can be deployed in hospitals and home healthcare settings to clear the air of infected bioaerosol droplets. Additionally, our products comply with all CARB regulations related to air cleaners for sale in California, and the Company’s manufacturer is registered with the State of California CARB.

Grand View Research: The global air purifier market size was estimated at USD 15.94 billion in 2023 and is expected to grow at a CAGR of 7.1% from 2024 to 2030, reaching approximately USD 25.58 billion by 2030.

Kronos can now provide schools, healthcare facilities, businesses, hotels, and government agencies with the best medical-grade air purification and air disinfection technology.

“As air quality concerns continue to rise globally, we are proud to announce that our manufacturer has been granted an additional FDA clearance for the Model 8 Air Purifier. We want to thank the FDA Team for their investigation and test results review of Kronos® CORE patented air disinfection technology,” said Greg Rubin, Interim CEO of Kronos. “We have been developing air disinfection and purification technology since 2002 and are experts in Indoor Air Quality. The recently approved FDA 510(k) clearance of the Model 8 device, powered by our patented Kronos® air disinfection technology, represents another major step forward in marketing our products to hospitals, doctors’ offices, allergy sufferers, and areas affected by natural disasters like wildfires.”

“There are only a few air purifier manufacturers on the market today that have received multiple 510(k) clearances, and this marks a significant milestone for our company and our shareholders. This certification validates the performance of the Kronos® Model 8 air disinfection technology capabilities as we prepare to manufacture our innovative products domestically and lead the air purification industry,” added Rubin.