Laon Ortho— 510(k) K250198

Substantially Equivalent

Laon Medi, Inc.

FDA 510(k) clearance K250198 for Laon Ortho, Substantially Equivalent on 2025-04-23. Applicant: Laon Medi, Inc.. Device class: 2.

Clearance details

Applicant: Laon Medi, Inc.
Product code: Code PNN
Device class: Class 2
Regulation: 21 CFR 872.5470
Advisory panel: Dental
Date received: 2025-01-23
Decision date: 2025-04-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Gwacheon-Si, KR

Download summary PDF View on FDA.gov ↗

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