Precision Digital Planning
Case data, clinical goals, revisions and approvals are managed through a controlled digital workflow.
ORYALIGN brings Shape Memory Aligners, surgical guide production and clinician-focused digital case management together in one system.
ORYALIGN · ADVANCED DENTAL PRODUCTIONCase data, clinical goals, revisions and approvals are managed through a controlled digital workflow.
Case-specific clear aligner solutions supported by advanced digital production.
Physical surgical guides produced after a digital implantology planning workflow.
Planning, revision, production and delivery communication stays within each case.
Every case is managed independently with its clinical records, planning history, approvals, communication and production status.

A clear-aligner service combining digital planning, case assessment, clinician approval, controlled production and delivery.

Case-specific surgical guide planning and physical production for digital implantology workflows.
ORYALIGN is structured to integrate digital orthodontics, implantology and advanced dental production into the clinician’s daily workflow.
Every case remains recorded, traceable and approval-driven from file review through production and delivery.
Controlled planning and production decisions.
A visible case journey from assessment to delivery.
Direct case-based communication with ORYALIGN.
Recorded approval, production and quality steps.
File validation, approved version control, production tracking and pre-shipment quality checks form one shared operating standard.
Case records and the correct file version are checked before production.
Critical production does not begin before the required plan approvals.
The approved product enters its defined manufacturing workflow.
The product and case contents are checked before shipment.
Shipment information remains visible in the clinician portal.
The clinician selects the product and securely uploads the required clinical records.
The ORYALIGN team evaluates the files, objectives and production requirements.
A clinical and technical scope is prepared for the clinician’s review.
The orthodontic or surgical-guide workflow is prepared for the selected product.
Only an approved case enters the controlled production workflow.
Final checks, packaging and shipment tracking are completed through the portal.
Patient records, files, assessment, plan approval, communication, production and shipment are managed through one case screen.