SPECIALIST RESTORATIVE CAD
Implant CAD Design
Restorative implant design begins with the exact component workflow, not just an implant brand. Pristine supports laboratories and restorative teams with implant crowns, bridges and related CAD work, scoped around supplied records and approved instructions.
Discuss this case typeWHO THIS SUPPORTS
A clear fit for your workflow.
Labs managing implant cases alongside routine production; practices with an in-house lab that needs component-aware design support.
Scope is confirmed for the specific indication, software and production route before acceptance.
Records to prepare
- Restorative prescription, tooth positions and intended retention approach
- Upper and lower scans, bite record and scan-body captures
- Exact implant platform, scan body, restorative component and library version
- Tissue scan and reference restoration where available; material and manufacturing instructions
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.
Confirm the component chain
Match the physical scan body to the digital library and planned restorative component. A familiar brand name is insufficient when platform, connection or component generation differs. Uncertain identification needs confirmation from the submitting team before design.
Design around the restorative envelope
Review the supplied tissue record, available space, contours and planned access. Contours are developed within the approved brief and component constraints. A design view cannot establish clinical tissue behavior or prove passive fit.
Review before manufacture
Check component assignments, intended retention, access position and production constraints. Deliver the agreed mesh or native case format. The lab and treating clinician retain manufacturing and clinical approval.
COMMUNICATION & REVISIONS
A traceable handoff.
Confirm implant platform, scan-body identity and component library before design. The submitting team resolves an uncertain component match; a familiar brand name alone does not close that question.
A changed scan body, component or retention plan can invalidate an earlier approval. Name the replacement information in one revision brief and reconfirm the required output.
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