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FDA Breakthrough Device Designation

Turning Medical Imaging into
ActionableAI Intelligence

Advancing the Future of Endoluminal Diagnostics and Therapeutics.

BSI Certification

ISO 13485:2016 & EN ISO 13485 • Certified by BSI

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Incubated & Supported By

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Our Vision

GI Cancers
Global Health Crisis

Global Burden

1 in 4
Cancer cases
1 in 3
Cancer deaths
Most patients are diagnosed only when symptoms emerge often at advanced, unresectable stages.

The Diagnostic Gap

Detection still depends heavily on human perception under intense time pressure leading to missed lesions and delayed intervention.

Early Gastric Cancer
upto 18%
lesions indicative of early gastric cancer missed
Early Esophageal Cancer
upto 25%
lesions indicative of early esophageal cancer missed
Why Early Detection Matters

From Late Stage to Early Cure.

When identified early, GI cancers are highly treatable through minimally invasive endoscopic procedures resulting in significantly better prognoses and reduced healthcare burden.

20%
5-Year Survival With late-stage detection
90%
5-Year Survival With early detection
Regulatory Status
CDSCO Test License
Form MD 13
Granted - July 2024
2x
FDA Breakthrough Device Designations
Expedited regulatory review
Reduced pre-market data requirements
Priority access to direct, frequent communication with the FDA
Reimbursement advantage, driving faster adoption through early insurance coverage
Real-Time Detection and Characterization

The Second Pair of Eyes for every endoscopic procedure.

Intelligent Workflow

From live video to final structured report.

Lesion Detection and Characterization

Real-time detection of early stage cancerous lesions, supporting morphological assessment aligned with the Paris Classification.

Landmark Recognition

Automatic identification of endoscopic station points ensures complete mucosal coverage and accurate photodocumentation.

Automated Reporting

Voice-to-text and intelligent mapping instantly generating ready to print standardized PDF reports.