meddevicedb.com FDA Device Reference

G-BLOCK

K253236 Class II Abbreviated
Decision Date
2025-09-29
Sponsor / Applicant
Graphenano Dental S.L.

Technical Specification

510(k) Submission ID K253236
Product Code EBF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3690
Decision Date 2025-09-29
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

G-BLOCK received FDA 510(k) clearance under submission number K253236, sponsored by Graphenano Dental S.L.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2025-09-29.

Classification & Regulation

This clearance is catalogued under FDA product code EBF and 21 CFR 872.3690, within the Dental review panel as a Class II device.