meddevicedb.com FDA Device Reference

Digital Intraoral X-Ray Sensor

K230811 Class II Special
Decision Date
2023-04-21
Sponsor / Applicant
Iray Imaging Technology (Haining) Limited

Technical Specification

510(k) Submission ID K230811
Product Code MUH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.1800
Decision Date 2023-04-21
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Digital Intraoral X-Ray Sensor received FDA 510(k) clearance under submission number K230811, sponsored by Iray Imaging Technology (Haining) Limited. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2023-04-21.

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.