SkinSmart Antimicrobial HydroGel
K-Number: K254041 · 2026-09-11
Device Summary
Frequently Asked Questions
What is the SkinSmart Antimicrobial HydroGel?
SkinSmart Antimicrobial HydroGel is a medical device that received FDA 510(k) clearance on 2026-09-11. The listed applicant is Magic Science Supply, LLC. The 510(k) number is K254041.
When did SkinSmart Antimicrobial HydroGel receive FDA 510(k) clearance?
SkinSmart Antimicrobial HydroGel received FDA 510(k) clearance on 2026-09-11, under 510(k) number K254041.
Who is the listed applicant for SkinSmart Antimicrobial HydroGel?
The FDA 510(k) record lists Magic Science Supply, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SkinSmart Antimicrobial HydroGel?
The FDA product code for SkinSmart Antimicrobial HydroGel is FRO. This falls under the Anesthesiology category.
Related Devices (Code: FRO)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.