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Evidence-informed perspectives on recurrent vaginal infections, microbiome
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We are pleased to welcome @Lara Zibners, MD as an Advisor to Cern.
Dr. Zibners is Co-Founder and Chairman of Calla Lily Clinical Care and a long-time advocate for innovation in women’s health. As a physician and entrepreneur operating across the U.S. and Europe, she brings a global lens to commercialization strategy and platform growth. The women’s health medical device ecosystem is collaborative and interconnected.
HITLAB x Cern Partnership Announcement
New York, NY – November 5, 2025 — HITLAB, a global leader in digital health innovation and evidence generation, today announced a strategic partnership with Cern Corporation, Inc., a pioneering women’s health technology company headquartered in Southern California. The collaboration aims to advance a groundbreaking, non-drug treatment for vaginal infections
FAQ
Your questions, answered.
Vaginal infections are common. Talking about them shouldn’t be hard. Here you’ll find
clear, evidence-informed answers to the questions women actually ask.
1. What is the Cern Device™?
The CernDevice™ is a platform technology comprised of intravaginal device which emits low level, visible, microbicidal light and is paired with our proprietary gel which facilitates placement as well as enhances the action of the microbicidal light.
2. Is it FDA-approved?
The CernDevice™ is not FDA cleared at this time and is not for sale in the U.S. nor internationally at this time.
3. How is this different from antibiotics or antifungals?
A Different Approach to Vaginal Infection Treatment…Traditional treatments for vaginal yeast infections and bacterial vaginosis rely primarily on antifungal or antibiotic drugs. Cern is developing a fundamentally different approach.
The Cern Device™ uses localized low level, visible spectrum, microbicidal light rather than systemic drugs to target pathogens directly at the site of infection. The technology is being developed to address both fungal and bacterial pathogens, including drug-resistant strains, through a physical, light-mediated mechanism. Because treatment is localized, Cern’s approach is designed to reduce many of the challenges associated with repeated drug therapy, including systemic drug exposure, drug–drug interactions, antimicrobial resistance, and the need for different drugs to treat yeast versus bacterial infections.
Cern is ultimately developing the technology as a provider-directed, at-home treatment—giving women a potential new option for recurrent vaginal infections that is convenient, localized, and non-systemic.
One technology. Yeast and bacteria. No systemic drugs.
This “visible light” has been indicated as safe on vaginal mucosal tissue.
4. Does it harm beneficial bacteria?
Designed with the Vaginal Microbiome in Mind
A healthy vaginal microbiome depends on a balanced microbial community, or state of symbiosis, that includes beneficial bacteria—particularly Lactobacillus species such as L. crispatus. Disruption of this balance, or dysbiosis, is associated with vaginal conditions such as bacterial vaginosis (BV) and vulvovaginal candidiasis (VVC).
Cern’s microbicidal-light treatment is being developed to reduce disease-associated bacterial and fungal pathogens while supporting preservation of beneficial vaginal bacteria. Because the antimicrobial effect is dependent on treatment parameters, including light dose and exposure duration, the technology may provide an opportunity to establish a therapeutic window that effectively reduces targeted pathogens while minimizing effects on beneficial organisms.
Cern’s laboratory testing suggests that key beneficial bacteria such as L. crispatus may demonstrate greater resilience to certain treatment conditions than disease-associated pathogens. This is particularly relevant because Lactobacillus-dominant vaginal communities, including those dominated by L. crispatus, are generally associated with vaginal health, while their depletion is frequently associated with vaginal dysbiosis.
This potential differential response may allow Cern’s treatment parameters to be optimized to reduce pathogenic microbial burden while limiting disruption of beneficial vaginal flora—an important consideration for women experiencing recurrent vaginal infections.
Rather than simply treating an infection, Cern’s approach is being developed with the broader vaginal microbial ecosystem in mind, with the goal of treating disease while supporting the conditions associated with a healthy, balanced vaginal microbiome.
5. Can it be used at home?
Cern’s treatment will debut as a prescriptive which is authorized by your healthcare provider. Cern’s treatment is designed for use at home, as needed, when needed, based on familiar recurrent symptoms. Please always consult your physician prior to use.
6. Who may be eligible for clinical studies?
Cern’s clinical studies will be in distinct geographic area/s here in the U.S.
If interested in participating in a Cern Clinical study, please inquire at Info@CernDevice.com
Disclaimer: The Cern Device™ is in clinical development and not FDA-cleared or approved. Information on this website is provided for
educational purposes only and should not be interpreted as evidence of clinical efficacy.