meddevicedb.com FDA Device Reference

Neodent Implant System - Zirconia Implant System

K210336 Class II Traditional
Decision Date
2021-08-13
Sponsor / Applicant
Jjgc Industria E Comercio DE Materiais Dentarios S.A.

Technical Specification

510(k) Submission ID K210336
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2021-08-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Neodent Implant System - Zirconia Implant System received FDA 510(k) clearance under submission number K210336, sponsored by Jjgc Industria E Comercio DE Materiais Dentarios S.A.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2021-08-13.

Classification & Regulation

This clearance is catalogued under FDA product code DZE and 21 CFR 872.3640, within the Dental review panel as a Class II device.