meddevicedb.com FDA Device Reference

White Endoseal MTA

K212229 Class II Special
Decision Date
2021-08-13
Sponsor / Applicant
Maruchi

Technical Specification

510(k) Submission ID K212229
Product Code KIF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3820
Decision Date 2021-08-13
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

White Endoseal MTA received FDA 510(k) clearance under submission number K212229, sponsored by Maruchi. The device was reviewed via the Special 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 KIF and 21 CFR 872.3820, within the Dental review panel as a Class II device.