meddevicedb.com FDA Device Reference

IPS Style Ceram, IPS Style Ceram One, IPS Style Press

K152103 Class II Traditional
Decision Date
2016-05-20
Sponsor / Applicant
Ivoclar Vivadent, AG

Technical Specification

510(k) Submission ID K152103
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 2016-05-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IPS Style Ceram, IPS Style Ceram One, IPS Style Press received FDA 510(k) clearance under submission number K152103, sponsored by Ivoclar Vivadent, 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 2016-05-20.

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.