Bright Cavity Liner— 510(k) K253248

Substantially Equivalent

Dmp Dental Industry S.A.

FDA 510(k) clearance K253248 for Bright Cavity Liner, Substantially Equivalent on 2026-01-13. Applicant: Dmp Dental Industry S.A.. Device class: 2.

Clearance details

Applicant: Dmp Dental Industry S.A.
Product code: Code EJK
Device class: Class 2
Regulation: 21 CFR 872.3250
Advisory panel: Dental
Date received: 2025-09-29
Decision date: 2026-01-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Markopoulo, GR

Download summary PDF View on FDA.gov ↗

Recent devices under product code EJK

K261728 — One-Fil LC2026-07-21
K230270 — 3M VitCal Liner/Base2023-02-06
K212475 — Prevest Denpro Cavity Liners (Apacal ART, Cal LC, Calcigel, CalUltra)2022-05-13
K201799 — CleaniCal2021-02-12
K202413 — LC ResinCal PC2020-11-20

More clearances from Dmp Dental Industry S.A.

K252469 — MAGNABOND SE; MAGNABOND UNIVERSAL; MAGNABOND UNIVERSAL DCA2025-11-06
K192830 — Bright Temporary C&B2020-09-02

Data sourced from openFDA. This site is unofficial and independent of the FDA.