SPECIALIST RESTORATIVE CAD
Removable & Denture CAD Workflows
Removable work needs a clear handoff between clinical records, setup review and production. Pristine helps laboratories scope denture and removable CAD cases without treating every indication as the same file-export task.
Discuss this case typeWHO THIS SUPPORTS
A clear fit for your workflow.
Removable labs needing supplemental design capacity or help coordinating a defined digital handoff.
Scope is confirmed for the specific indication, software and production route before acceptance.
Records to prepare
- Case-specific prescription and clinician-approved design requirements
- Relevant arch and bite records
- Existing denture/setup references when supplied
- Required tooth and base outputs, libraries and production process
- For partial/framework work: the prescribed design and supported component workflow
Use an agreed case-transfer route. The public inquiry form is for business details, not patient files.
ACTUAL DESIGN WORK
A view into the detail.
Representative work from the approved Pristine portfolio. CAD views show design work and do not establish clinical outcomes or the scope of a future case.
Explore the portfolio
WORKFLOW & REVIEW
From the brief to the handoff.
Scope the indication first
Complete dentures, partial dentures and frameworks have different record and design requirements. Confirm that the specific workflow is supported before submission. Do not infer framework prescriptions or clinical support requirements from scans alone.
Separate records from approvals
Name the record set and version used for the setup. Capture approval of the design stage before producing final files, particularly when reference dentures and new scans are both present.
Validate production compatibility
Confirm how teeth, base and any framework output will be manufactured or assembled. The receiving lab verifies supported materials and tooling. Unsupported workflows remain out of scope until confirmed.
COMMUNICATION & REVISIONS
A traceable handoff.
Name the removable indication and the supported design scope first. A denture arrangement and a partial framework have different record and component dependencies.
List affected framework, tooth or base elements rather than sending an unqualified reset request. Confirm any change to the manufacturing route before replacing approved outputs.
Scope, file formats, delivery target and revision terms are agreed before work starts. Your team retains clinical and manufacturing approval.
Build a lab-preference packetA DEFINED FIRST STEP
Discuss the work.
Define the handoff.
One paid test case, quoted to scope. Delivery target and revision terms agreed before work starts.
Request a test-case quote