every patient is unique, their cancer treatment should be too

Kallisio creates personalized precision solutions for oncology.
Stentra™ — our first FDA cleared and CE marked device — is available now.

one size does
not fit all

when treatment isn’t built for the individual, patients pay the price

Generic, one-size-fits-all medical devices can’t account for each patient’s individual anatomy. The result: less precise treatment, avoidable side effects, and outcomes that fall short of what’s possible.

In head and neck cancer radiation therapy, for example, the consequences are well documented: painful mouth sores (mucositis), difficulty swallowing, treatment interruptions.

precision care built around the individual, not the average patient

At Kallisio, every solution we develop starts with the same principle – that effective treatment means accounting for each patient’s unique anatomy, not defaulting to one-size-fits-all. We’re building a pipeline of patient-specific solutions across oncology, each designed to reduce avoidable harm and improve outcomes.

Stentra™ is our first solution, and it’s already changing outcomes in head and neck radiation therapy.

  • tech-enabled precision anchoring
  • custom-fit by design, guided by data
  • built for seamless clinical integration
  • backed by reimbursement pathways

Flagship product

Stentra™ custom 3D-printed immobilization device for a sub-millimeter precision fit

In the News

Patient-Ready Personalization for Precision Therapy…

New Ebook

Advancing Precision in Head & Neck Cancer Treatment…

easily integrate precision into your treatment workflow

Capture your patient data

Step 1
1
Receive your patient-specific solution
Step 2
2
Treat your patient
Step 3
3

scalable innovation, one
patient at a time

  • Engineered by oncology and medtech leaders
  • Powered by intelligent digital infrastructure
  • Proven in real-world clinical settings
  • Trusted by global healthcare partners
ACCC
AMS
Materialise
Nurelm
Myrava
Salesforce

gain up to 2–3 hours* per patient in workflow efficiency

The Stentra™ System improves efficiency by reducing simulation setup time and speeding up treatment planning. A patient-precision fit ensures easy reproducibility, minimizing delays and increasing accuracy.

*calculated from several clinical studies we can share

stentra™ is our first solution, it won't be our last

Kallisio is developing a pipeline of patient-specific oncology solutions each built on the same principle of precision personalized care. If you’re a clinician, partner, or investor interested in what’s coming next, we’d like to hear from you.

ready to bring precision care to your patients?

Join the cancer centres already using Stentra™ — Kallisio’s first FDA and CE cleared solution for head and neck radiation therapy. Our team will respond within 24 hours.

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Radiation Oncologist Details

Stentra™ is FDA cleared and prescribed (Rx) by the Radiation Oncologist. To build a Stentra device, we need to know how the Radiation Oncologist wants to position the patient's tongue. We also need the patient's target simulation date to ship Stentra™ in time for planning. Once we have the information outlined in this form and the required oral optical scans, the Stentra™ device can be delivered in as little as 72 hours. Please review the Stentra™ types below and fill out the following information:

Stentra™ types

If you are not the patient's Radiation Oncologist but are placing this order on their behalf, we need your information as well.

Radiation Oncologist Details

Stentra™ is FDA cleared and prescribed (Rx) by the Radiation Oncologist. To build a Stentra device, we need to get the order and prescription from the patient's radiation oncology team. We also need the patient's target simulation date to ship Stentra™ in time for planning. Once we have the required oral optical scans, the Stentra™ device can be delivered in as little as 72 hours. Please provide the following information:

Case approval

Providing Additional Information

If you would like, you can download and print out our brochure found on our patient page under « talk to your doctor ». Please bring this brochure to your Radiation Oncologist and ask them to look into whether this is a good option for your case.

Your dental practice

Your Radiation Oncologist

Your dental practice or provider equipped with an intraoral optical scanner

What happens next

Thank you for submitting the order request. When this form is submitted, if you provided an email to us, we will dispatch an onboarding invite to the radiation oncology clinic via email requesting that they register their practice and authorize the order for your patient. If no email was provided, please call the patient's radiation clinic to get them onboard and fill out an order form through our website.

What happens next:

  1. Review instructions. Detailed scan protocols and submission instructions will be emailed to the addresses associated with your dental clinic listed in your request.
  2. Continue with the scan. If all dental work has been done and the patient is cleared to start radiation therapy, continue with the scan following the instructions sent to you.
  3. Oncology setup. Once the radiation oncology team completes their setup, authorizes and confirms the order, we can start fabricating the device.

Thank you for your partnership in getting this patient ready for treatment.

Billing Information

Reimbursement information — for reference only. This is not billing advice and does not guarantee coverage or payment. Providers are responsible for code selection, documentation, and claim accuracy.

CPT® 77334 (Treatment devices, design and construction; complex) covers complex radiation therapy devices designed and fabricated for an individual patient. Physician involvement in device selection, design, and placement should be documented.

Stentra™ is an FDA 510(k) cleared (K232293), patient-specific intraoral positioning device. Providers may consider CPT 77334 for its design and construction, subject to their own coding review.

Delivery method: the code is not limited to one technique and may apply across IMRT, 3D-CRT, and other external beam approaches.

Multiple devices: when a thermoplastic mask and Stentra™ each serve a distinct, documented purpose, each may be separately reportable, subject to NCCI edits, MUE limits, and payer policy.

Questions: contact Kallisio at care@kallisio.com. For coding decisions, consult your coding and compliance team.

Financial Responsibility, Prescription & Accuracy Attestation

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Attestation to Truthful Information

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