Surgical residency programs
A scored simulation for one procedure, with results sent to the program's evaluation records.
Surgical teams ask for headsets to do three different jobs: rehearse a procedure, study a patient's anatomy before the case and see images during it. Each job has its own data, sign-off and regulatory weight. Agnotic Technologies builds the software for the job you choose, on headsets your team already uses.
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Virtual reality surgery software is the headset application and imaging pipeline behind surgical simulation, preoperative planning from a patient's own CT or MRI, and augmented reality overlays in the operating room. Agnotic Technologies builds it as a services engagement and settles each use case's data source, device status and clinical sign-off before the first scene is built.
The headset is rarely the problem. Projects stall on ownership, data and the line between a training tool and a device.
A demo scene impresses the department, but nobody wrote the scoring rules, so the program director cannot use the results in an evaluation.
Planning models are built by hand in a 3D tool for each case, and the file lives on one person's laptop instead of in the patient's imaging study.
Segmentation from a routine CT protocol is too coarse for small structures, and surgeons stop opening the model after the first few cases.
The app is written against one headset vendor's SDK, so a hardware change means starting again.
An overlay prototype slowly gains guidance features until it makes a device claim nobody decided to make.
Simulation scores stay inside the app and never reach the residency program's evaluation records.
The three use cases share a headset and little else. We fill in this table with the clinical owner before scoping, because the input data and the device status decide most of the build.
| Use case | Input data | Output | Likely FDA status | Clinical owner | Failure that stops adoption |
|---|---|---|---|---|---|
| Training simulation | Synthetic anatomy and a procedure broken into steps; no patient data | Scored attempts per resident: step order, time, errors and instrument path | Usually a training product when it makes no claim about a patient; confirm with your regulatory lead | Program director and teaching faculty | Scores that faculty do not agree with, so nobody uses them |
| Preoperative planning | The patient's own CT or MRI series pulled from PACS | A segmented 3D model the surgeon reviews on a headset or desktop | Image processing with segmentation or 3D visualization for patient management fits 21 CFR 892.2050, Class II | Operating surgeon, with radiology | A model the surgeon cannot correct or does not trust |
| Intraoperative AR overlay | The approved planning model, registered to the patient in the room | Images overlaid on the surgical field during the case | A medical device; plan for FDA premarket review before clinical use | Surgeon, with biomedical engineering and the device maker's quality team | Registration drift and line of sight problems in a live room |
Three rules apply to every surgical XR build, whichever use case you start with.
Training, planning or guidance is agreed in writing first. The claim sets the device path, the validation work and who signs off, so features cannot drift into guidance later.
Planning models are derived from DICOM and stored back as DICOM objects that reference the source series, so a model travels with the study instead of a shared drive.
Step order, time, errors and instrument path are defined with the teaching faculty, and pass criteria are their decision, set as configuration rather than code.
We build the surgical software around the headset. VR therapy, rehab and headset fleet tools are covered on our VR healthcare software page.
Step-based scenes for a defined procedure, with branches for common errors and faculty-set pass criteria.
Step order, time per step, errors and instrument path recorded for each attempt and kept per resident.
Attempts and scores by resident, procedure and date, with an export to the residency evaluation system.
CT or MRI series to labelled structures and surface meshes, with correction tools for radiology and the surgeon.
The patient model on a headset or desktop: rotate, slice, measure and review it together at a case conference.
Segmentations and models stored back to PACS as DICOM objects linked to the source study.
Registration workflow and overlay rendering for device teams, built under their design controls and quality system.
OpenXR as the runtime interface, so one surgical app can run on conformant headsets from more than one vendor.
This is the image to model pipeline we start from. Each step leaves a record, so the team can see which series, which labels and whose approval produced the model in the headset.
A DICOM query fetches the ordered series from PACS. Protocol checks such as slice thickness and contrast phase run before any processing, and a study that fails them is sent back with a reason.
Automated or semi-automated labelling produces a DICOM Segmentation object that references the source images and shares their frame of reference.
Radiology or the surgeon edits labels in the viewer. Approval is recorded with the person's name and the time, and only approved labels move on.
Surface meshes are generated from the approved labels and simplified for the headset, keeping the original resolution for desktop review.
The mesh is saved as an Encapsulated STL object in the same study, so the model sits in the patient's imaging record with the series it came from.
The planning viewer opens the model through the study reference. Notes and measurements from the case conference are saved against the same case.
Choices we make with your team for surgical builds. Engines and devices for therapy apps are listed on our VR healthcare page.
Status views we build into the program director and planning dashboards.
By procedure and date, against the faculty schedule.
Attempts that met the faculty pass criteria, step by step.
Planning models approved before the case date.
Whether the operating surgeon opened the model before the case.
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Teams we scope surgical XR work with, and where each one usually starts.
A scored simulation for one procedure, with results sent to the program's evaluation records.
A repeatable pipeline from CT to approved model, replacing hand-built files for each case.
An AR overlay or planning prototype built under the maker's design controls for its own submission.
Shared procedure libraries for several departments, with one scoring model.
A first module and a clear claim, so the company knows its regulatory path before it raises on a demo.
Planning models from the patient's imaging, reviewed at the case conference before surgery.
The systems a surgical XR build reads from and writes to.
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Our architectures are built to handle massive data loads and user bases, keeping performance steady whether you're serving ten or ten million.
Using our suite of internal tools and proven frameworks, we cut setup work so your first release reaches users sooner.
Beyond simple wrappers, we build deep-learning integrations and predictive analytics directly into the core of your industry-specific workflows.
We start with one use case and one procedure or case type. Timing depends on your data and devices, and we agree a fixed first release on the scoping call.
Use case, procedure, headsets in use and who signs off clinically.
The use case table filled in, the device path agreed and the imaging or rubric inputs confirmed.
One scene or one model on the real device, reviewed by faculty or the surgeon.
Scoring and dashboard, or the planning pipeline, live for one procedure or case type.
More procedures, more case types and support under agreed change control.
Short facts we design around, each linked to its primary source.
A medical image management and processing system is a Class II device under 21 CFR 892.2050, and its advanced functions may include image segmentation, multimodality image registration and 3D visualization for interpretation and patient management.
Source: 21 CFR 892.2050 (eCFR)The DICOM Segmentation IOD stores a classification of pixels in one or more referenced images as binary, fractional or label map segmentations, and shares the Frame of Reference of the images it was derived from.
Source: DICOM PS3.3, section A.51 Segmentation IODDICOM defines an Encapsulated STL IOD that describes a 3D model in Stereolithography format encapsulated within a DICOM object, so a planning model can be stored with the patient's imaging study.
Source: DICOM PS3.3, section A.85 Encapsulated 3D Manufacturing Model IODsThe OpenXR specification describes OpenXR as the interface between an application and an XR runtime, which may handle frame composition, peripheral management and raw tracking information.
Source: Khronos Group, OpenXR 1.1 Specification, section 1.1We don't just build products; we forge lasting partnerships. See how we've helped industry leaders transform their vision into technical reality.

“I can clearly see how Agnotic has a unique way of handling end-to-end development. They are always active on quick chat and provide support quickly.”
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Founder, My Lauren
This page covers surgical simulation, planning and overlays. These pages cover the work around it.
Pain distraction, motor rehab, exposure therapy and headset fleets.
Simulated patient conversations for clinical education.
Software for surgical practices and their clinical workflows.
Image storage, viewing and DICOM workflows behind planning models.
Scheduling and documentation choices for surgical services.
Explore other production-grade engineering platforms we deliver across healthcare.
The technical patterns behind this platform translate naturally into adjacent verticals.