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510(k) clearance

Dia-X Sil Light Body

FDA 510(k) source

510(k) number
K254152
Applicant
DiaDent Group International
Decision date
Sep 16, 2026
Date received
Dec 22, 2025
Decision
Substantially Equivalent
Clearance type
Traditional
Product code
ELW
Device type
Material, Impression
Device class
Class II
Regulation
21 CFR 872.3660
Advisory committee
Dental
Statement or summary
Summary
Third party
N
Location
Cheongju-Si, KR