NTI Splint is a custom dental laboratory product in the Times Dental Lab occlusal splints range. The NTI Splint is designed to reduces muscle activity and is intended to relieve temporomandibular joint pain. 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 NTI Splint 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
Reduces muscle activity and is intended to relieve temporomandibular joint pain.
Indications
Muscle spasm, temporomandibular joint pain, and tension headaches.
Relative contraindications
Anterior crossbite or missing anterior teeth.
Instructions for use
Wear on the upper anterior teeth at night and avoid posterior contact.
Case planning
For every NTI Splint, 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.
