01
Report understanding
Explain the labels, measurements, and stated limitations in an approved device report.
Industry
Medical Devices
Connect device output, supporting records, and understandable education in a human-reviewed medical AI workflow.
What Lunas supports
- Readable explanations around device reports and terminology
- Context across device output, labs, symptoms, and records
- Human review and escalation kept visible
The opportunity
Why this work needs medical context
A device can produce an accurate measurement while leaving the user unsure what it means, whether a change matters, or who should review it. Support teams also need to distinguish product questions from clinical and safety concerns.
Lunas can become the explanation and context layer around device data. Stethos can help organize permitted reports and approved education, while future governed integrations can connect device workflows to Lunas without presenting the model as the device, the clinician, or the final authority.
Where Lunas fits
Useful work before the final decision
Stethos helps explain, organize, and investigate. People and qualified professionals stay responsible for the decisions that follow.
02
Longitudinal context
Place compatible measurements beside laboratory values, symptoms, and history when permitted.
03
Customer education
Help users understand setup, terminology, and the right next support channel.
04
Responsible escalation
Send technical, adverse-event, or clinical concerns to the designated human team.
A practical workflow
From a question to human review
A repeatable path makes the model easier to supervise and the result easier to trust.
- 01
Define intended use
Separate education and support from regulated clinical functionality.
- 02
Ground approved content
Use cleared product information, report definitions, and escalation rules.
- 03
Assist the user or agent
Explain and summarize without making unsupported clinical claims.
- 04
Review and monitor
Keep human approval, safety reporting, quality checks, and change control in the loop.
Product path
Start with Lunas today. Grow into governed workflows.
Lunas.One is available to individuals today. Team & Enterprise workspaces and a governed Stethos API are in active development — the roadmap below is directional, not a promise of present availability, and larger deployments will require the right privacy, security, evaluation, and human-review controls.
Available in Lunas
- Upload and discussion of supported reports
- Medical-context explanations through Stethos 1.0
- Charts for compatible, reviewed observations
Team, Enterprise & API direction
- Team & Enterprise support and review workflows
- Broader device-data visualizations
- Governed APIs for approved device integrations
Questions
What people usually want to know
Is Lunas itself a medical device?
Lunas is positioned as AI-assisted information and organization, not diagnosis or treatment. A specific integrated use may require separate regulatory analysis based on its intended use and claims.
Can device data be imported automatically today?
Current workflows center on supported user-provided files and records. Direct integrations belong to the governed API roadmap.
Can Stethos handle adverse-event reports?
It may assist with organizing information, but regulated safety intake and reporting require validated processes and responsible human teams.
Try the product
Bring one real health question into context.
Use Lunas for information and organization, then involve a qualified professional whenever a health decision is needed.