News

PathPresenter Achieves Key 510(k) Regulatory Milestone

We’re thrilled to share that portfolio company PathPresenter has received FDA 510(k) clearance for its Clinical Viewer, a diagnostic-grade digital pathology platform designed to aid pathologists in reviewing and interpreting whole slide images. This clearance marks a major step forward in PathPresenter’s mission to improve access to high-quality, diagnostic digital pathology tools worldwide.

Unlike traditional solutions, the Clinical Viewer builds on PathPresenter’s established, widely used platform, now bringing those capabilities into regulated clinical workflows with greater confidence, security, and interoperability.

Congratulations to the entire PathPresenter team on this achievement!

Press Release