Souldent follows structured quality control procedures throughout the laboratory workflow, from receipt of the case through design, manufacture, finishing, final inspection, and dispatch. Each case is checked against the submitted prescription, clinical instructions, materials requested, and the information supplied by the referring dental practice.

Our products are developed and produced under quality management processes designed to support accuracy, reliability, traceability, and compliance with applicable medical device requirements. Quality checks are carried out at key stages of production so that each restoration can proceed only when it meets the required technical standard.

Incoming impressions, models, intraoral scans, and supporting records are reviewed before production begins. Where a concern is identified that may affect fit, function, shade, occlusion, or the final clinical result, Souldent may contact the practice before proceeding.

During production, Souldent uses case tracking, batch numbering, and case management processes to support traceability. Where required, the manufacturing history of a case can be reviewed internally to assist with quality assurance, remake assessment, or guarantee review.

Finished cases are examined before release to the customer. This final inspection is intended to confirm that the work corresponds with the prescription and that the restoration has been completed to Souldent’s expected standard of craftsmanship and precision.