meddevicedb.com FDA Device Reference

CERAMICS2IN1

K100150 Class II Traditional
Decision Date
2010-05-25
Sponsor / Applicant
Biodenta Swiss AG

Technical Specification

510(k) Submission ID K100150
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 2010-05-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CERAMICS2IN1 received FDA 510(k) clearance under submission number K100150, sponsored by Biodenta Swiss AG. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2010-05-25.

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.