Sensilift Pro (ST300XXYYZZZ)— 510(k) K250341

Name: FDA 510(k) clearance K250341
Creator: U.S. Food and Drug Administration
Published: 2026-01-06

Substantially Equivalent

El Global Trade, Ltd.

FDA 510(k) clearance K250341 for Sensilift Pro (ST300XXYYZZZ), Substantially Equivalent on 2026-01-06. Applicant: El Global Trade, Ltd.. Device class: 2.

Clearance details

Applicant: El Global Trade, Ltd.
Product code: Code PAY
Device class: Class 2
Regulation: 21 CFR 878.4420
Advisory panel: General, Plastic Surgery
Date received: 2025-02-06
Decision date: 2026-01-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Netanya, IL

Download summary PDF View on FDA.gov ↗

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