Approved-plan intake
Case files and approved design outputs are organized with the order information needed for production coordination.
Private-label production workflow
DBT Technology supports dental organizations that need a structured path from professionally approved aligner plans to coordinated OEM clear aligner production. The service is designed for business-to-business programs, with project scope, responsibilities and production requirements confirmed before implementation.
Discuss your requirementsOEM clear aligner manufacturing is the operational part of a private-label aligner program. It covers how approved digital plans, order data, production instructions and partner requirements move through a controlled workflow. DBT works with dental groups, laboratories, distributors and aligner brands according to an agreed project scope.
The treating dental professional remains responsible for diagnosis, prescription, treatment decisions and final plan approval. Manufacturing begins only after the required professional review and approval have been completed.
Case files and approved design outputs are organized with the order information needed for production coordination.
Material, staging, packaging, labelling and delivery requirements are reviewed during program setup and confirmed where available.
Defined contacts and status checkpoints help dental and laboratory teams manage questions, revisions and order handoffs.
Requirements vary by collaboration, but onboarding commonly covers digital plan formats, approved staging files, arch segmentation, order identifiers, quantities, labelling, packaging and delivery instructions. Regulatory and market-access responsibilities must also be allocated clearly between the participating organizations.
If treatment design is still required, review the separate Invisible Aligner Treatment Design service. Organizations developing a broader private-label offer can review the OEM Invisible Aligner Brand Program.
This page focuses on the production workflow after professional approval. Treatment-design support focuses on preparing a staged digital plan for professional review. Keeping these steps separate makes responsibilities clearer and helps prevent unapproved design information from being treated as a production instruction.
It is intended for dental groups, laboratories, distributors and aligner brands seeking a business-to-business production workflow. Suitability and capacity are reviewed during project scoping.
No. The qualified treating dental professional reviews and approves the treatment plan. DBT's manufacturing workflow uses the approved information supplied for production.
Yes. Private-label packaging and labelling requirements can be reviewed during onboarding. Feasibility, responsibilities and the final scope must be confirmed for each program.
The exact specification is agreed during onboarding and may include approved staging outputs, production files, order identifiers and packaging instructions.
A production-focused workflow may be discussed when complete, professionally approved plans and compatible production information are supplied.
This service is intended for dental organizations and professional business partners. Diagnosis, prescriptions, treatment decisions and final case approval remain with the qualified dental professional responsible for the patient.
Discuss your requirements