meddevicedb.com FDA Device Reference

S-Plant Dental Implant System

K231429 Class II Traditional
Decision Date
2023-12-18
Sponsor / Applicant
Idis Co., Ltd.

Technical Specification

510(k) Submission ID K231429
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2023-12-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

S-Plant Dental Implant System received FDA 510(k) clearance under submission number K231429, sponsored by Idis 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 2023-12-18.

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.