meddevicedb.com FDA Device Reference

JET BITE; JET BLUE BITE FAST; JET BLUE BITE SUPERFAST

K250969 Class II Abbreviated
Decision Date
2025-06-27
Sponsor / Applicant
Dent4you AG

Technical Specification

510(k) Submission ID K250969
Product Code ELW
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3660
Decision Date 2025-06-27
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

JET BITE; JET BLUE BITE FAST; JET BLUE BITE SUPERFAST received FDA 510(k) clearance under submission number K250969, sponsored by Dent4you AG. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2025-06-27.

Classification & Regulation

This clearance is catalogued under FDA product code ELW and 21 CFR 872.3660, within the Dental review panel as a Class II device.