meddevicedb.com FDA Device Reference

Multi-Unit DAS System

K243732 Class II Traditional
Decision Date
2026-01-29
Sponsor / Applicant
Talladium España, SL

Technical Specification

510(k) Submission ID K243732
Product Code NHA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3630
Decision Date 2026-01-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Multi-Unit DAS System received FDA 510(k) clearance under submission number K243732, sponsored by Talladium España, SL. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2026-01-29.

Classification & Regulation

This clearance is catalogued under FDA product code NHA and 21 CFR 872.3630, within the Dental review panel as a Class II device.