GreenLight OSMedical Device Licensing
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Fast-Track Your Regulatory Journey

Join the GreenLight OS Pilot Program to unlock comprehensive regulatory roadmaps, expert guidance, and lifetime benefits.

One-time payment • Money-back guarantee

Full Document Matrix

Unlock the complete, itemized list of documents required for your specific device submission (510(k), MDL, etc.), plus applicable standards.

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Expert Review Session

Get a complimentary 30-minute strategy call with a regulatory specialist to review your classification and discuss next steps.

Unlimited Classifications

Run as many assessments as you need for different devices or variations across US and Canada markets.

Everything You Get for $99

Comprehensive Regulatory Roadmap

Know exactly what to submit. We identify your pathway (e.g., 510(k), De Novo) and list every required document.

Consensus Standards List

Access the specific ISO and IEC standards applicable to your device type to ensure compliance.

Grandfathered Pricing

Lock in this early-adopter rate. You'll receive a lifetime discount on future enterprise subscriptions.

Priority Feature Voting

Direct line to our product team. Tell us what to build next (e.g., EU MDR, Automatic Drafter).

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