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Xenex Makes De Novo Petition to FDA re. LightStrike UV room disinfection technology
Xenex Disinfection Services, a world leader in UV disinfection technology for healthcare facilities, has filed a De Novo petition with the US Food & Drug Administration for medical device market authorisation of its LightStrike+ ultraviolet room disinfection technology.
The company's patented device uses a xenon lamp to create broad spectrum UV light intended to quickly destroy pathogens on surfaces in healthcare facilities.
Xenex's LightStrike technology is currently being sold pursuant to an FDA enforcement policy that was issued to allow light-based disinfection products to be brought to market during the pandemic (Enforcement Policy for Sterilizers, Disinfectant Devices and Air Purifiers During the Coronavirus Disease 2019 (COVID-19) Public Health Emergency).
The De Novo pathway allows for creation of an entirely new product classification - and, if granted, will strengthen Xenex's enviable position in the UV disinfection industry by obtaining FDA authorisation to market LightStrike+ (the new iteration of the device) as a medical device. The filing includes substantial data on testing with the device and leverages the robust scientific evidence published in peer-reviewed articles about the efficacy of the LightStrike disinfection technology.
Harmful microorganisms can remain on surfaces in healthcare facilities, even after the best manual cleaning efforts. Many of the world's leading hospitals and health systems, including HonorHealth, Mayo Clinic, MD Anderson, Ochsner Health and Texas Health Resources, utilise LightStrike's powerful UV-C disinfection technology to achieve optimal cleanliness by destroying pathogens missed during the manual room cleaning process.
There have been more than 45 peer-reviewed, published studies in scientific journals demonstrating the effectiveness of the LightStrike disinfection technology, which is protected by 193 patents.
"When we started Xenex, UV room disinfection in healthcare facilities was novel," says Dr Mark ‘Tuck’ Stibich, founder and chief scientific officer of Xenex. “Over the course of time, proactive hospitals deployed our robots to disinfect their facilities and we're extremely proud of the success those hospitals achieved.
“Today, room disinfection with LightStrike robots has become standard of care in many hospitals. The value and importance of what they've accomplished is such that we are submitting our De Novo petition to the FDA and we welcome the change in the UV room disinfection industry because it's that important to patients and healthcare workers
Xenex CEO, Morris Miller adds: "LightStrike Germ-Zapping Robots have been deployed by more than 1,000 hospitals worldwide and we're very proud that those hospitals have safely completed more than 35 million disinfection cycles.
"We have been working closely with the FDA to describe to them our unique broad spectrum UV disinfection device, and we're very excited to pursue this De Novo classification. Our hospital partners have been looking for clarity in the UV room disinfection market and we believe that this will help them make informed, evidence-based decisions."
Healthcare professionals strive to make hospitals safe and for their facilities to be sanctuaries for healing. Ensuring a properly disinfected environment is a key part of that strategy. The LightStrike UV robot emits intense bursts of broad spectrum, pulsed xenon UV light to destroy pathogens on surfaces and is effective against multi-drug resistant organisms found in hospitals, including methicillin-resistant Staphylococcus aureus (MRSA), Clostridioides difficile (C. diff), and VRE (Vancomycin-resistant Enterococci).
Frost & Sullivan named Xenex the 2020 Global Company of the Year for its patented technology and being at the vanguard of the fight against SARS-CoV-2 (the virus that causes Covid-19).
9th February 2023