meddevicedb.com FDA Device Reference

Dental Cone-beam Computed Tomography (mDX-15P Series)

K261748 Class II Traditional
Decision Date
2026-07-23
Sponsor / Applicant
Hefei Meyer Optoelectronic Technology, Inc.

Technical Specification

510(k) Submission ID K261748
Product Code OAS
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1750
Decision Date 2026-07-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Dental Cone-beam Computed Tomography (mDX-15P Series) received FDA 510(k) clearance under submission number K261748, sponsored by Hefei Meyer Optoelectronic Technology, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2026-07-23.

Classification & Regulation

This clearance is catalogued under FDA product code OAS and 21 CFR 892.1750, within the Radiology review panel as a Class II device.