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Data and alignment review
Review of the submitted DICOM and surface data, file integrity, anatomy, alignment, and technical readiness for the agreed workflow.
Dental implant planning & surgical guide design
Implant planning and guide design that fits your team's workflow.
PlanSurg supports dental laboratories, clinics, and surgical teams with implant-planning and surgical-guide design capacity. The technical work is integrated with the provider-review, restorative, production, and communication pathways defined for the engagement.
Scope shaped around the case
From focused implant cases to more complex guided workflows.
Support can be defined for single implants, partially edentulous cases, multiple-implant cases, full-arch workflows, stackable systems, bone-reduction pathways, and selected complex implant-planning needs.
Case acceptance depends on the intended scope, available data, software and instrumentation requirements, production pathway, and the responsibilities each party is prepared to assume. A technical service description does not replace case review or clinical approval.
Planning and design support
Defined technical work, prepared for responsible professional review.
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Implant-planning support
Technical planning support based on the objectives, implant system, restorative information, anatomical constraints, and review pathway provided by the responsible team.
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Surgical-guide design
Guide configuration and design prepared around support, fixation, access, instrumentation, planned use, and the manufacturing requirements defined for the engagement.
A four-stage public workflow
Data. Plan. Approval. Release.
Data: the technical dataset and engagement requirements are reviewed before work proceeds.
Plan: the planning and design work is prepared within the defined scope and software environment.
Approval: the appropriately licensed provider reviews and approves the clinical plan and the design intended for clinical use.
Release: controlled deliverables are released to the laboratory, clinic, printing center, or qualified manufacturer responsible for the next step.
For dental laboratories
Additional capacity behind your brand.
PlanSurg can support an agreed portion of planning and guide-design work while the laboratory maintains its client relationship, restorative workflow, production pathway, and communication structure.
For clinics and surgical teams
Support without replacing the ecosystem you trust.
Planning and design support can be integrated with the software, laboratory, restorative partner, and production resources already used by the practice.
For developing workflows
Connect planning with a practical production pathway.
For teams building an in-house or hybrid guide workflow, PlanSurg can help define responsibilities, data requirements, review steps, documentation, training needs, and the boundary between internal and external production.
Clinical authority and manufacturing
Clear responsibility at every handoff.
The appropriately licensed provider remains responsible for diagnosis, indication, treatment objectives, implant selection, final implant positioning, patient consent, clinical decisions, surgery, and clinical outcomes.
PlanSurg is responsible for the technical scope it accepts, including planning or design work, file integrity, version control, documentation, identified inconsistencies, and the release controls defined for the engagement.
Manufacturing remains with the laboratory, clinic, printing center, or qualified manufacturer contractually responsible for production. PlanSurg does not manufacture implants or custom plates.
A practical first conversation
Start without sending patient information.
Tell us about the organization, case types, current workflow, software environment, production pathway, and the capacity or implementation problem you are trying to solve. Patient files and protected health information are not required for an introductory discussion.
Start a professional inquiry