meddevicedb.com FDA Device Reference

General Cutting Straight

K230106 Class I Traditional
Decision Date
2023-05-24
Sponsor / Applicant
Nakanishi, Inc.

Technical Specification

510(k) Submission ID K230106
Product Code EGS
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4200
Decision Date 2023-05-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

General Cutting Straight received FDA 510(k) clearance under submission number K230106, sponsored by Nakanishi, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2023-05-24.

Classification & Regulation

This clearance is catalogued under FDA product code EGS and 21 CFR 872.4200, within the Dental review panel as a Class I device.