Quality Control Flow
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01
Case Intake Review
Prescription, tooth number, material, shade, implant system and required records are reviewed before production.
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02
Scan or Impression Review
Margins, occlusion, contact data, scan completeness and impression quality are checked according to case type.
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03
CAD Design Review
Margin, cement space, connector dimensions, emergence profile and design consistency are reviewed when applicable.
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04
Material Verification
Material brand, product reference and batch information can be documented for applicable cases upon request.
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05
In-Process Inspection
Milling, sintering, staining, glazing, denture setup, framework processing and finishing are checked during production.
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06
Final QC
Fit, margin, occlusion, proximal contact, shade, surface finishing, polish, cleanliness and prescription consistency are reviewed.
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07
Shipping Verification
Packaging, labels, shipment information and tracking details are checked before dispatch.
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08
Issue Review and Remake Handling
Reported issues are reviewed against the prescription, files, production information and finished restoration.
What Each Quality Stage Protects
Before Production
The intake and record review stage identifies missing prescriptions, unclear margins, incomplete bite data or unconfirmed implant details before irreversible work begins.
During Design
Design review focuses on the restoration geometry that can affect fit, contacts, occlusion, connector strength, emergence profile and cleanability.
During Production
Material and in-process checks help keep the finished case aligned with the confirmed material, design and customer instructions.
Before Dispatch
Final inspection and shipping verification check the completed restoration, prescription match, cleanliness, labels and protective packaging.
Customer Information That Supports Better QC
- Complete prescription and consistent tooth numbering
- Clear scans or impressions, opposing arch and bite records
- Shade references and clinical photos when esthetics matter
- Exact implant system, platform and scan body details
- Written approval requirements for complex design stages
- Prompt clarification when the laboratory reports an open question
Review a Representative Case
Send a representative case and its quality priorities so the required records, checkpoints and approval stages can be discussed before production.