meddevicedb.com FDA Device Reference

Digital Intraoral X-ray Imaging System

K212279 Class II Traditional
Decision Date
2021-10-07
Sponsor / Applicant
Iray Technology Taicang , Ltd.

Technical Specification

510(k) Submission ID K212279
Product Code MUH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.1800
Decision Date 2021-10-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Digital Intraoral X-ray Imaging System received FDA 510(k) clearance under submission number K212279, sponsored by Iray Technology Taicang , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2021-10-07.

Classification & Regulation

This clearance is catalogued under FDA product code MUH and 21 CFR 872.1800, within the Dental review panel as a Class II device.