meddevicedb.com FDA Device Reference

DENSEO FAIRY

K082158 Class II Traditional
Decision Date
2008-10-15
Sponsor / Applicant
Xpdent Corp

Technical Specification

510(k) Submission ID K082158
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 2008-10-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DENSEO FAIRY received FDA 510(k) clearance under submission number K082158, sponsored by Xpdent Corp. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2008-10-15.

Classification & Regulation

This clearance is catalogued under FDA product code EIH and 21 CFR 872.6660, within the Dental review panel as a Class II device.