Dorsal Appliance is a custom dental laboratory product in the Times Dental Lab orthodontic related products range. The Dorsal Appliance is designed to advances the mandible to open the airway. The appliance is manufactured from the dentist's prescription and the clinical or digital records provided for the case.
Who this product is for
This page is for dentists, orthodontists, and dental laboratories comparing appliances for a defined treatment plan. The Dorsal Appliance description organizes the clinical application, indications, relative contraindications, instructions, and professional-use limitations into self-contained sections. This structure helps clinicians review the product and helps search and answer systems identify the correct appliance entity without relying on unsupported claims.
Clinical application
Advances the mandible to open the airway.
Indications
Snoring and mild to moderate obstructive sleep apnea.
Relative contraindications
Severe obstructive sleep apnea or temporomandibular joint disorders.
Instructions for use
Increase advancement gradually to reduce discomfort.
Case planning
For every Dorsal Appliance, the prescribing clinician should assess the dentition, periodontal condition, skeletal pattern, occlusion, tooth position, soft tissues, temporomandibular joints, oral hygiene, patient cooperation, and treatment objective. The design and activation or wear schedule must follow the approved prescription. Appliance categories are not automatically interchangeable because fixed and removable designs place different demands on anchorage, compliance, hygiene, adjustment, monitoring, and maintenance.
Laboratory and quality context
Times Dental Lab is a full-service dental laboratory in Shenzhen, China, established in 2008. The catalog states that more than ten experienced orthodontic technicians handle products ranging from retainers to functional appliances and clear aligners. It also states that the wider laboratory has more than 400 experienced technicians, FDA establishment registration number 3008727912, continuous ISO compliance, and the use of CE-, FDA-, and ISO-approved materials. These details give company-level production and quality-system context; the product-specific information above remains the factual basis for evaluating the appliance.
Professional use notice
This content is for professional reference and does not replace diagnosis or individualized treatment planning. A qualified clinician remains responsible for patient selection, contraindication assessment, prescription approval, fitting, activation, monitoring, hygiene instructions, adjustments, and follow-up care.
