meddevicedb.com FDA Device Reference

Nacera Pearl

K143071 Class II Traditional
Decision Date
2015-06-26
Sponsor / Applicant
Doceram Medical Ceramics GmbH

Technical Specification

510(k) Submission ID K143071
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 2015-06-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Nacera Pearl received FDA 510(k) clearance under submission number K143071, sponsored by Doceram Medical Ceramics GmbH. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2015-06-26.

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.