Company and Stock Identity

How Digital Diagnostics Connects to the Public Market

Company structure
Private company
Market access
No current public listing was verified.
Research focus
This is one of the few products that makes a diagnosis without a physician reading the image, so the questions are about responsibility rather than accuracy alone. Two clearances sit under the applicant name Digital Diagnostics in this site's FDA records, K203629 from 2021 and K213037 from 2022, and the company says the exam is reimbursable under CPT code 92229. Ask who signs the result, what happens on an ungradable image, and who refers the patient on.

No ownership change was found. Checked on 2026-10-10 against the company's own newsroom, where the 2025 and 2026 items are clinic deployments and outside coverage rather than a sale or a listing.

Open the public company market data feed for the full directory, ownership relationships, stock identifiers, and dated snapshots.

First-Hand Company News

Latest Developments

... Digital Diagnostics ... Company source

A Utah clinic used Digital Diagnostics' eye AI and referred a quarter of patients

Digital Diagnostics said on 25 November 2025 that The People's Health Clinic in Utah, which serves uninsured residents of Summit and Wasatch counties, is using LumineticsCore to screen patients with diabetes for eye disease. The company says the clinic completed nearly 100 eye exams in about three months and that roughly 25 percent of those patients were identified for urgent referral to an ophthalmologist.

Why it matters: A one in four urgent referral rate is high, and the honest reading is that it says as much about the population as about the software: a clinic serving uninsured patients is likely seeing people whose diabetes has gone unwatched for years. That is exactly where moving the exam into the building changes outcomes, because the barrier was never the reading, it was the second appointment. Nearly 100 exams is a small start, and the figures are the company's own, so a larger clinic should ask for referral rates from sites that look like its own patient mix.

See company developments across the healthcare AI market.

Careers and Qualifications

What to Know Before Applying

Work areas: The careers page is built around a general application rather than named roles, and lists Coralville in Iowa and Austin in Texas as offices alongside remote work. It describes the team as computer scientists and clinicians.

Qualification signal: An autonomous diagnosis carries more regulatory and liability weight than a flag for a radiologist, so people who have taken that kind of claim through the FDA, or who understand primary care billing, matter more here than general imaging experience.

Check current roles at Digital Diagnostics. A careers page is the source of record for openings. This profile does not claim a role is open unless the company lists it now.

Related Healthcare AI Roles

Training to Compare

Buyer Snapshot

Best-fit buyer
Radiology leadership, pathology leadership, clinical informatics, imaging IT, patient safety, and procurement
Primary use case
Triage studies, flag findings, support image interpretation, and coordinate time-sensitive care
Typical deployment
Usually integrated with PACS, RIS, worklists, or digital pathology systems and monitored inside the clinical workflow

Evidence questions

  • Was the tool tested prospectively and independently on comparable equipment and patients?
  • What are sensitivity, specificity, false positive workload, and time-to-action effects?
  • How does performance vary by site, scanner, demographic subgroup, and disease prevalence?

Regulatory and workflow questions

  • Which FDA authorization covers the exact product version, modality, and intended use?
  • Who retains final clinical responsibility and how is disagreement with the AI handled?
  • What post-deployment monitoring and material update notification does the vendor provide?

Data and contract questions

  • Where are images and derived data processed and retained?
  • Which PACS, RIS, pathology, and EHR integrations are supported in production?
  • Can data be used for model improvement, and what controls govern secondary use?

Evidence and Regulation

FDA Clearances on Record

Digital Diagnostics appears on 2 cleared products in the federal 510(k) record, across 1 device type.

A clearance means the FDA agreed the product is close enough to something already on the market to be sold for that use. It is not a finding that the product helps patients, and it is not a ranking against anything else on this page. A company is linked to an FDA clearance only when the 510(k) applicant name on the government record is confirmed by hand to be that same company, including former corporate names. Name similarity alone is never enough, and rejected matches are listed below with the reason.

What the Published Research Says About This Work

Independent studies on the work itself help separate category evidence from one company's claims.

First-Hand Sources