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Business · 02/12/2003Updated: 10/17/2026 · 1 min read

FDA Classifies Dental Sonography Device and Jaw Tracking Device for Diagnosis of Temporomandibular Joint Disorders

Summary

The FDA has classified the dental sonography device and jaw tracking device into Class I and Class II, respectively, for use in diagnosing temporomandibular joint disorders and associated orofacial pain. The agency has also made a guidance document available to serve as the special control for these devices.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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