meddevicedb.com FDA Device Reference

EDS Bioceramic Sealer (Bioseal)

K202281 Class II Traditional
Decision Date
2021-02-12
Sponsor / Applicant
Essential Dental Systems

Technical Specification

510(k) Submission ID K202281
Product Code KIF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3820
Decision Date 2021-02-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EDS Bioceramic Sealer (Bioseal) received FDA 510(k) clearance under submission number K202281, sponsored by Essential Dental Systems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2021-02-12.

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.