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Experience regulatory clarity in 30 seconds. See your device classification with full rule traceability.

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Choose the regulatory jurisdiction for your medical device

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Built for manufacturers. Audited for regulators.

How It Works

Experience regulatory clarity in three simple steps

01
📄

Answer Simple Questions

Answer a few targeted questions about your device. Each step references the exact regulation.

02

See the Logic Build

Watch in real-time as Greenlight OS applies regulatory rules to determine your classification.

03

Get Your Report

Download a complete report with classification, applicable rules, and next steps.