1 in 7Americans lives with a medical implantMeet the WilhelmAI team at Booth 1312 — AHRA 2026, July 12–14 · Orlando, FL$2.5Bin MRI revenue lost to implant uncertainty each yearWatch WilhelmAI on YouTube — subscribe for early access content40MMRI procedures performed in the U.S. annuallyFollow WilhelmAI on LinkedIn for product updates, clinical insights, and company news4,500+implants in the database with direct OEM documentation1 in 7Americans lives with a medical implantMeet the WilhelmAI team at Booth 1312 — AHRA 2026, July 12–14 · Orlando, FL$2.5Bin MRI revenue lost to implant uncertainty each yearWatch WilhelmAI on YouTube — subscribe for early access content40MMRI procedures performed in the U.S. annuallyFollow WilhelmAI on LinkedIn for product updates, clinical insights, and company news4,500+implants in the database with direct OEM documentation
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Resources

Everything behind the platform

The thinking, evidence, and answers behind WilhelmAI. Start with the white paper, then find quick answers to what technologists, clinical teams, and administrators ask us most.

Featured

White Paper

The Platform That MRI Safety Has Been Missing

By Tony Oropeza, Founder & Chairman, WilhelmAI LLC. Practicing MRI/CT/XR Technologist.

Why implant safety has been left to scattered PDFs for too long, and how an end-to-end platform built on MRI Safety Intelligence™ closes the gap, from primary-source IFU extraction to daily regulatory monitoring and defensible documentation.

Patient guide

Video walkthrough

MRI patient guide

A practical patient-facing overview you can share with staff or families before MRI safety review.

Education

Video · 2 min

MR Conditional, Explained

The most misread label in MRI safety — what “MR Conditional” actually means, why the conditions are non-negotiable, and what happens when even one is missed.

Frequently Asked Questions

Platform basics

What is WilhelmAI, and who is it for?

WilhelmAI is an end-to-end MRI Implant Safety Platform built on MRI Safety Intelligence™, designed by a practicing MRI technologist. It brings a verified device library, AI and advanced search, the Active Implant Tool, one-click reporting, a CPT® reimbursement layer, and daily QA into one system. It serves the people who carry MRI safety, technologists, radiologists, and MR safety officers, along with the departments and networks behind them.

How do I use it?

Three ways. With AI search, type as much as you know in plain language and WilhelmAI narrows it down, no exact spelling required. With advanced search, filter by manufacturer, model family, and field strength when you already know the device. With the Active Implant Tool, work through generator-to-lead configurations for cardiac, neurostimulator, and other active implants that need more than an RF limit.

What does it tell me about a device?

Whether a device is MR Safe, MR Unsafe, or MR Conditional, and for conditional devices the actual conditions, not just the label, field strength, maximum SAR, spatial gradient, slew rate, RF and coil restrictions, lead requirements, programmer steps, and scan duration limits where the manufacturer specifies them. Every answer links to the source it was built from.

How many devices are in the library?

Over 4,500 verified entries spanning dozens of manufacturers, growing continuously. Every entry is built from primary-source manufacturer documentation by our own team and QA'd daily.

How do I know the information is accurate?

Every entry is sourced from official manufacturer Instructions for Use and regulatory documentation, then manually reviewed and verified by experienced technologists. WilhelmAI is not a web scraper. The Watchtower then monitors regulatory and manufacturer sources daily, so when labeling changes or a recall posts, the affected entries are flagged for review before the next clinician queries them.

What sets it apart

What are the Active Implant Tool and the Watchtower?

The Active Implant Tool is a structured reference for the implants that drive the most cancellations, cardiac rhythm devices, neurostimulators, spinal cord stimulators, and deep brain stimulators, with generator-to-lead matching, per-pairing scan parameters, implant location, coil restrictions, and prep, all sourced from the manufacturer IFU. The Watchtower is the automated monitoring layer that runs daily and flags condition changes and recalls against the affected entries, so what you search reflects what was true overnight rather than a year ago.

Can it generate reports and support CPT® reimbursement?

Yes. One click generates a structured device report from the same sourced data, and radiologists and MR safety officers can document their risk analysis directly in it. WilhelmAI also holds an AMA CPT® licensing agreement and maps screening work to the 2025 code set, CPT® 76014 through 76019, delivering the documentation and audit trail that billing starts from. WilhelmAI does not submit claims; the department and its billing team decide what is reportable.

CPT® is a registered trademark of the American Medical Association.

Safety, data, and compliance

Does WilhelmAI make the clinical decision?

No. WilhelmAI does not own any medical device data and does not make clinical decisions. It is a research and reference tool that organizes and cites verified information. The safety determination and all clinical judgment remain the sole responsibility of the technologist or clinician in practice.

How is patient data handled, and is IT integration required?

WilhelmAI is built with zero PHI storage by design. It does not collect, store, or transmit protected health information. Because of that, and because it is web-based, a department can start without a lengthy IT or security review. No integration is required to begin.

Where does the device data come from?

From four cited categories. Manufacturer and regulatory sources such as device IFUs, FDA labeling, and recall notices are the primary authority, supported by professional society guidelines, peer-reviewed literature, and clearly labeled expert consensus where published evidence is limited. The sourcing is always visible.

Access and getting started

Is it available now, and what does it cost?

WilhelmAI is live and in clinical use across five countries, the United States, Australia, Canada, Switzerland, and the United Kingdom. It is an annual subscription priced by scanner volume, with network and enterprise licensing for larger systems and volume discounts at scale. Trials are available. Reach out through the contact form for pricing tailored to your facility.

How do I get a demo or trial?

Two ways. Fill out the demo form and our team will follow up, or at your convenience. Either path walks through the full feature set. Ask about a trial when you reach out if you want to evaluate WilhelmAI in your own environment.

Requests and support

How do I request a device, suggest a feature, or ask something else?

Send it through the contact form. The library grows continuously and we welcome device requests, feature ideas from working clinicians shape the platform directly, and we follow up on other questions within one business day.