
NeoGenix Biosciences builds the next generation of sperm selection and analysis tools for the IVF lab. Our commercial product, SpermSearch.AI, helps embryologists find viable sperm in severely compromised samples and testicular tissue โ in use across 32 paying clinics in 10 countries, with A$300k+ ARR in under twelve months. Our second product, SpermGuide, is a microfluidic device with peer-reviewed evidence showing 82โ92% reduction in DNA fragmentation versus standard of care.
Male factor is implicated in roughly half of all infertility cases, yet the dominant sperm preparation technique โ density gradient centrifugation โ was developed in the 1980s and is now known to inflict significant DNA damage on the very cells embryologists most need to be healthy. In the hardest cases (cryptozoospermia, surgical testicular samples) embryologists can spend hours manually scanning slides for a handful of viable sperm, often unsuccessfully. The IVF lab toolkit hasn't materially changed in decades, even as the science has moved on.
SpermSearch.AI is an AI co-pilot for embryologists that scans samples and surfaces candidate sperm, dramatically cutting search time on the hardest cases โ including testicular tissue. SpermGuide is a single-use microfluidic device that uses biomimetic flow to isolate high-DNA-integrity sperm without centrifugation; published clinical data shows an 82โ92% reduction in DNA fragmentation versus standard DGC. Together they give IVF clinics a hardware-plus-software pathway to better outcomes for the patients existing techniques fail.
The global ART market sits at a combined TAM of US$758m across two products. SpermSearch.AI addresses ~6,188 ART laboratories globally at US$10โ15k per seat annually (TAM: US$186m); SpermGuide addresses ~2.88 million fresh IVF cycles per year at US$60โ90 per device (TAM: US$572m).
Raising up to AUD 1.5M Seed at AUD 8M post-money, deployed against: (1) SpermSearch.AI TGA Class I clearance and international sales scale-up; (2) SpermGuide manufacturing lock-down for commercial launch; and (3) ongoing clinical validation.

