meddevicedb.com FDA Device Reference

Dental Cone-beam Computed Tomography (FinScan F350)

K242805 Class II Traditional
Decision Date
2025-01-09
Sponsor / Applicant
Changzhou Finno Medical Technology Co., Ltd.

Technical Specification

510(k) Submission ID K242805
Product Code OAS
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1750
Decision Date 2025-01-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Dental Cone-beam Computed Tomography (FinScan F350) received FDA 510(k) clearance under submission number K242805, sponsored by Changzhou Finno Medical Technology Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2025-01-09.

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.