MAGNABOND SE; MAGNABOND UNIVERSAL; MAGNABOND UNIVERSAL DCA— 510(k) K252469

Name: FDA 510(k) clearance K252469
Creator: U.S. Food and Drug Administration
Published: 2025-11-06

Substantially Equivalent

Dmp Dental Industry S.A.

FDA 510(k) clearance K252469 for MAGNABOND SE; MAGNABOND UNIVERSAL; MAGNABOND UNIVERSAL DCA, Substantially Equivalent on 2025-11-06. Applicant: Dmp Dental Industry S.A.. Device class: 2.

Clearance details

Applicant: Dmp Dental Industry S.A.
Product code: Code KLE
Device class: Class 2
Regulation: 21 CFR 872.3200
Advisory panel: Dental
Date received: 2025-08-06
Decision date: 2025-11-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Markopoulo, GR

Download summary PDF View on FDA.gov ↗

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