MEDILIGHT— 510(k) K231952

Substantially Equivalent

Medicreations, LLC

FDA 510(k) clearance K231952 for MEDILIGHT, Substantially Equivalent on 2025-09-03. Applicant: Medicreations, LLC. Device class: 2.

Clearance details

Applicant: Medicreations, LLC
Product code: Code ONF
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 2023-06-30
Decision date: 2025-09-03
Decision: Substantially Equivalent
Clearance type: Special
Location: Las Vegas, NV, US

Download summary PDF View on FDA.gov ↗

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