For Manufacturers

Extend your implants' reach, without vendor lock-in

Salnus is a software-only, implant-agnostic preoperative orthopaedic planning AI. We give surgeons a vendor-neutral 3D planning surface, and manufacturers gain a planning and templating layer around their implant systems.

SUPPORTED IMAGING

CTMRIX-ray

DICOM inputs: CT, MRI, and X-ray are processed through a single pipeline.

THE MODEL

Software-only (no hardware, no manufacturing), browser-based, and implant-agnostic. Surgeons keep their implant choice, and your catalogue becomes one of the libraries the planner can target. The planning surface travels with the surgeon across institutions.

WORKFLOW

DICOM in (CT, MRI, X-ray), AI bone segmentation, 3D anatomy and measurements, then a preoperative plan and OR-ready outputs. Processing runs client-side in the browser, so patient images need not leave the clinic.

WHY IMPLANT-AGNOSTIC WINS FOR YOU

Surgeons resist single-vendor lock-in. A vendor-neutral planner is adopted more widely, which widens the set of cases where your implants are planned and chosen. Reach grows through agnostic distribution, not exclusivity.

ENGAGEMENT MODELS

Implant library integration
We integrate a manufacturer implant catalogue into the implant-agnostic preoperative planning pipeline.
Co-developed planning module
Manufacturer-specific preoperative planning and 3D templating built around your implant systems.
Per-case engineering (concierge)
Case-by-case preoperative 3D planning delivered to the surgeon and billed to the manufacturer.
Licensing & revenue-share
Commercial terms are scoped per partner.

WHAT STAYS PROTECTED

Because we are software-only, we do not manufacture implants or compete with yours. Client-side DICOM processing keeps patient data in the clinic (KVKK/GDPR-aligned). Our performance reporting is calibrated and transparent.

DISCUSS INTEGRATION

Leave a short note about your implant systems and the integration model you have in mind, and we will get back to you.

KVKK ✓ · GDPR ✓

Salnus products are research-use-only (RUO) and are not cleared or approved medical devices. The regulatory pathway (CE, TITCK) is navigated jointly.

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For Implant Manufacturers, Salnus