MEDILIGHT— 510(k) K231952

Substantially Equivalent

Medicreations, LLC

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

Clearance details

Applicant
Medicreations, LLC
Product code
Code ONF
Advisory panel
General, Plastic Surgery
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Las Vegas, NV, US
Download summary PDFView on FDA.gov ↗

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