Applied Photonix Launches ViroZap®, the First FDA-Cleared Medical Device for In-Duct Air Disinfection

Applied Photonix Launches ViroZap®, the First FDA-Cleared Medical Device for In-Duct Air Disinfection
Press Release

Applied Photonix Launches ViroZap®, the First FDA-Cleared Medical Device for In-Duct Air Disinfection

News provided by Applied Photonix Sep 15, 2026, 08:49 ET Originally distributed via PR Newswire

Hospital-grade air disinfection technology now available for homes, schools, offices, and healthcare facilities - integrating directly into existing HVAC systems

Applied Photonix today announced the commercial launch of ViroZap®, the first FDA-cleared, Class II medical device engineered for in-duct air disinfection. Unlike standalone air purifiers, ViroZap integrates directly into new or existing HVAC systems, delivering continuous, whole-building air treatment without the need for room-by-room units.

ViroZap was developed by Dr. Yogi Goswami, Distinguished University Professor at the University of South Florida and a member of the Florida Inventors Hall of Fame.

ViroZap Scales from Households to Hospitals
ViroZap Scales from Households to Hospitals

Proven Performance, Third-Generation Technology

Built on third-generation plasmonic photonic technology, ViroZap treats recirculated air continuously and at low energy cost. The device does not use UV-C light, which can cause retinal damage and burn the skin. Some UV-C systems also produce ozone, which can irritate the lungs. ViroZap uses safe, UV-A light and does not produce ozone.

At an airflow rate of 500 CFM, independent testing confirms:

  • 99.9995% reduction of airborne RNA/DNA viruses
  • 99.9997% reduction of airborne bacteria (gram-positive and gram-negative)
  • 99.995% reduction of mold and fungal spores
  • Rapid VOC detoxification, with no ozone byproduct

Engineered for Real-World HVAC Integration

ViroZap is compliant with ASHRAE 241 and ASHRAE 170 standards and is pressure-drop neutral, operating seamlessly with our proprietary coated MERV 13 or 15 filters and a MERV 8 pre-filter. A HEPA filter coating option is also available, upon request. The system scales from single-family residential installations to large hospitals, schools, commercial buildings and institutional HVAC systems.

"ViroZap represents a fundamental shift in how we think about indoor air quality — from filtration alone to active, continuous disinfection at the source," said Terry Murray, Vice President of Sales & Marketing, Applied Photonix. "With FDA clearance as a Class II medical device, we're able to bring hospital-grade air safety to the spaces people spend the most time in: their homes, schools, offices, and of course, healthcare facilities."

Availability and Partnership Opportunities

ViroZap is now available for commercial deployment. Applied Photonix is actively seeking distribution and installation partners across the United States and internationally to support growing demand across residential, commercial, education, and healthcare markets.

About Applied Photonix

Applied Photonix develops advanced photonic technologies for indoor air quality and disinfection. Its flagship product, ViroZap®, is the first FDA-cleared, Class II medical device for in-duct air disinfection, delivering hospital-grade air treatment through existing HVAC infrastructure.

Media Contact & Partnership Inquiries: Terry Murray, tmurray@aphotonix.com, (828) 808-2955 direct mobile

SOURCE Applied Photonix

This press release was originally distributed on September 15, 2026 via PR Newswire. View the original release.

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FAQ

ViroZap® is the first FDA-cleared, Class II medical device engineered for in-duct air disinfection. Unlike standalone air purifiers, it integrates directly into new or existing HVAC systems, delivering continuous, whole-building air treatment without the need for room-by-room units. It was developed by Dr. Yogi Goswami, Distinguished University Professor at the University of South Florida and a member of the Florida Inventors Hall of Fame.

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At an airflow rate of 500 CFM, independent testing confirmed a 99.9995% reduction of airborne RNA/DNA viruses, a 99.9997% reduction of airborne bacteria (gram-positive and gram-negative), and a 99.995% reduction of mold and fungal spores. ViroZap also provides rapid VOC detoxification with no ozone byproduct.

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No. ViroZap does not use UV-C light, which can cause retinal damage and burn the skin, and some UV-C systems also produce ozone, which can irritate the lungs. ViroZap uses safe UV-A light and third-generation plasmonic photonic technology, and it does not produce ozone.

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Yes. ViroZap integrates directly into new or existing HVAC systems and is pressure-drop neutral, operating with Applied Photonix's proprietary coated MERV 13 or MERV 15 filters and a MERV 8 pre-filter. A HEPA filter coating option is also available on request. The system scales from single-family homes to large hospitals, schools, commercial buildings, and institutional HVAC systems, and it is compliant with ASHRAE 241 and ASHRAE 170 standards.

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Applied Photonix is actively seeking distribution and installation partners across the United States and internationally to support demand in residential, commercial, education, and healthcare markets. For partnership inquiries, contact Terry Murray, Vice President of Sales & Marketing, at (828) 808-2955, or reach out through the Applied Photonix contact page.

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