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Biogensis Implant System-Kisses

K142813 Class II Traditional
Decision Date
2015-07-31
Sponsor / Applicant
Biogenesis Co., Ltd.

Technical Specification

510(k) Submission ID K142813
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2015-07-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Biogensis Implant System-Kisses received FDA 510(k) clearance under submission number K142813, sponsored by Biogenesis Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2015-07-31.

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.