Locations
San Francisco, CA, USA
industry
Biotechnology
Stage
Seed
founded in
2025
We are building a unified biomedical testing and regulatory platform that connects every stage of product development from CAD design through simulation, bench testing, and verification to FDA Q-Submissions. You can think of us as Palantir for the biomedical industry. Currently, engineers, scientists, and regulatory teams work in isolated tools that don't communicate, forcing manual data recreation and documentation assembly. Our platform replaces this fragmented process with a single validated environment where simulated patient anatomy, test data, and requirements are all linked and traceable. It automates verification reporting, identifies missing tests, and generates compliant submission packages automatically, cutting months off development timelines and reducing regulatory risk.
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