
The AI co-pilot inside every interventional procedure. At the table for the coronary, the colon, the bronchus and the bile duct: it sees every frame, measures every lumen, and speaks only when it matters.
It sees every frame.
Not one procedure. Millions of them.
Annotated by the physicians who perform them.
Illustrative, generated imagery · not patient data
Illustrative scenario on a generated image.
Every modality in.
One intelligence.
Every lumen out.
of early oesophageal cancer lesions are missed at endoscopy
of early gastric cancer lesions are missed at endoscopy
cancer cases worldwide is gastrointestinal
cancer deaths worldwide is gastrointestinal
Published epidemiology, not neo performance data. Miss rates are upper bounds.
neo flags, measures and recommends. It never acts on the patient, and nothing it shows reads as an instruction.
Overlays live in the margins of the image. Nothing neo draws covers the region the operator is looking at.
Findings surface between acts: after an injection, at the end of a pullback, as the scope withdraws.
Unit, confidence and source frame travel with every value. A number without provenance is not shown.
When nothing is wrong, neo shows one steady aqua line. Calm is information too.
From the data it learns on to the console beside the operator. Each layer carries its own regulatory status, stated plainly.
Real-time detection of subtle early gastric and oesophageal cancers during white-light endoscopy, and angiography-derived physiology in the cath lab.
Endoscopy video, and co-registered angiography, IVUS, OCT and FFR, annotated by the physicians who perform these procedures.
Procedures become linked, de-identified, labelled records, with a rights ledger for every frame.
The intelligence rehearses thousands of procedures before it enters a real room. First room: the cath lab.
FDA · May 2024Breakthrough Device Designation for early gastric cancer detection
FDA · Dec 2024Breakthrough Device Designation for early oesophageal cancer detection
ISO 13485 ↗ISO 13485:2016 and EN ISO 13485, certified by BSI. Certificate MD 839871.
CDSCO · MD-13Test licence, India, granted July 2024. Registered prospective study live at Fortis.
BusinessWire India ↗RNT Health Insights receives FDA Breakthrough Device Designation for its early gastric cancer detection tool
BioSpectrum India ↗Second US FDA Breakthrough Device Designation, for the oesophageal cancer detection tool
Fortune India ↗Pfizer offers grant and incubation support to 14 Indian health-tech startups under its INDovation programme
The Economic Times ↗Nikhil Kamath unveils the first 15 grantees of his WTFund
MedTech Innovator ↗Named to the MedTech Innovator Asia Pacific Accelerator
The Economic Times ↗Pfizer to fund six startups through its INDovation programme for healthcare









