Test the intended receiving task
Interoperability is more than displaying a surface file. State what the receiver needs to do: inspect records, begin a design, continue an editable project or manufacture an output. Select an authorized exercise and define the context needed for that task.
The existing scanner-to-lab guide explains the overall handoff, and the file-role guide explains geometry versus native-project context. This page adds a bounded test protocol with recorded versions, expected observations and a receiving decision. It does not name universally compatible scanner/software combinations.
Freeze the configuration record
Record the acquisition application/release, scanner, export method, license option and receiving CAD environment. Preserve the original package. Record any changes as a separate trial, so a successful later run does not hide why the first failed.
3Shape’s July 31, 2024 support article documents STL/PLY export from accepted Dental Manager orders with the TRIOS Scan STL Export option enabled; it lists PLY export from Dental System 2021 onward. That is a scoped mechanism, not a blanket promise for every scanner portal. The DentalCAD overview says color display is available when scan data contains color information; confirm whether the actual transfer preserves what the receiver needs.
Use stage-specific acceptance observations
Agree the expected records with the receiving team before export. Record missing items and uncertain context explicitly; do not repair or reposition the source records simply to make a trial appear successful.
| Pilot checkpoint | Observation to record |
|---|---|
| Original package | Record roles, current brief and authoritative source |
| Transfer | Files/context actually received and omitted items |
| Import | Application result, errors and available objects |
| Interpretation | Identifiable reference roles, scale/orientation questions and appearance |
| Design stage | Intended task possible, blocked or requiring clarification |
| Save/output | Required saved state and receiver-accepted deliverable |
| Decision | Observed scope, limitations and review owner |
Record a bounded result, not a brand verdict
If export succeeds but the receiver lacks the intended reference, mark transfer observed and task blocked. Ask whether a different supported export or additional record is needed. Do not convert an import failure into a claim that a scanner is poor or that CAD can reconstruct missing information.
A hypothetical training trial may display geometry while the planned review also needs appearance information. Record the missing requirement and request the supported route; do not infer that a common filename extension guarantees it.
A successful trial validates the recorded task under its observed conditions. Returned design/native editing, production acceptance and other indications need their own checks when they are part of the proposed workflow. Revisit the pilot when software, entitlement or dependencies change. No clinical accuracy benchmark or Pristine integration is established by this blank protocol.
Louie validation and limits
Technical review pending — unverified locally. Louie and the acquisition/receiving teams must validate the exact scanner, release, export entitlement, record roles, receiving modules and observed result. No scanner-to-Pristine integration, numerical accuracy, color fidelity or complete round-trip compatibility has been tested or asserted.
The CSV is a blank operational worksheet with no patient data, executable code, configuration pack or clinical/manufacturing values. It does not perform an installation or authorize a production change. Examples in this guide are hypothetical, not measured results or approved Pristine case evidence.
Source notes
Official documentation checked October 6, 2026. Source dates and scope are listed below; a current source check does not establish applicability to every installed release. Original worksheets and decision frameworks require owner/administrator review.
Prepared by Pristine Dental Design · October 6, 2026. Actual prescriptions, applicable manufacturer instructions and responsible design/production approvals govern each case.