FDA DESIGNATES VAPORIZED HYDROGEN PEROXIDE (VHP) AS A CATEGORY A STERILIZATION METHOD, STREAMLINING MEDICAL DEVICE APPROVAL

In January 2024, the U.S. Food and Drug Administration (FDA) officially recognized vaporized hydrogen peroxide (VHP) as an Established Category A sterilization method for medical devices. This reclassification acknowledges VHP's long-standing safety and effectiveness, simplifying the regulatory process for manufacturers utilizing this sterilization technique. Understanding the FDA's Reclassification Previously categorized...

DELOX’S SOLID HYDROGEN PEROXIDE FORMULATION RECEIVES NON-HAZARDOUS CLASSIFICATION

Delox is excited to announce a pivotal regulatory milestone in bio-decontamination technology. Our solid hydrogen peroxide formulation (DeloxHP) has received official classification as non-corrosive and non-hazardous from the Department of Transportation (DOT), meaning it is not categorized under Organic Peroxides. This distinction simplifies our product’s transportation, as no additional safety...

DELOX TECHNOLOGY TO ELIMINATE MICROORGANISMS USING HYDROGEN PEROXIDE VAPOR RECEIVES SEED FUNDING

Kiilto Ventures, Caixa Capital and Bionova Capital invest in hydrogen peroxide vapor bio-decontamination company Delox. Bio-decontamination startup Delox secured € 750,000 of funding through a seed capital round of € 450,000 to which € 300,000 of public funding was added. This funding will finance the required steps to initiate product commercialization...

TACKLING THE COVID-19 OUTBREAK: A HYDROGEN PEROXIDE STERILIZATION APPROACH

As the COVID-19 pandemic is unfolding, Delox is finding a way to support the healthcare system in the fight against the infectious outbreak. Every hospital currently suffers a major shortage of protective equipment for the health personnel on the front line of the combat against the virus. As a result, there is...

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