meddevicedb.com FDA Device Reference

EMBRACE WETBOND CLEAR SEALANT

K052281 Class II Traditional
Decision Date
2006-02-08
Sponsor / Applicant
Pulpdent Corporation

Technical Specification

510(k) Submission ID K052281
Product Code EBC
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3765
Decision Date 2006-02-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EMBRACE WETBOND CLEAR SEALANT received FDA 510(k) clearance under submission number K052281, sponsored by Pulpdent Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2006-02-08.

Classification & Regulation

This clearance is catalogued under FDA product code EBC and 21 CFR 872.3765, within the Dental review panel as a Class II device.