LUOFUCON® Antimicrobial Wound Gel

FDA 510(k) K252028 · Huizhou Foryou Medical Co., Ltd.

Substantially Equivalent

510(k) numberK252028

Submission

Device name
LUOFUCON® Antimicrobial Wound Gel
Applicant
Huizhou Foryou Medical Co., Ltd.
Huizhou, CN
Received
June 30, 2025
Decision date
March 11, 2026
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FRO – Dressing, Wound, Drug
Device class
Unclassified

Other 510(k)s with product code FRO

510(k)DeviceApplicantDecision
K254041SkinSmart Antimicrobial HydroGelFRO · Traditional Magic Science Supply, LLC09/11/2026SE
K261646Redermax® Antibacterial Wound MatrixFRO · Traditional Beijing Kreate Medical Co., Ltd.08/14/2026SE
K253665Vashe Plus Antimicrobial SolutionFRO · Traditional Urgo Medical North America, LLC08/11/2026SE
K261023Microdacyn Wound Irrigation SolutionFRO · Traditional Sonoma Pharmaceuticals, Inc.06/24/2026SE
K251929SilverCeuticals® Antimicrobial Wound GelFRO · Traditional Silverceuticals, Inc.06/24/2026SE
K261638Bonvadis®FRO · Special Oneness Biotech Co., Ltd.06/17/2026SE
K254073StatSeal DiscFRO · Traditional Merit Medical Systems, Inc.05/13/2026SE
K254191IWD-Gel™FRO · Traditional InnovaCorium, Inc.04/07/2026SE
K252023MiraChlor Antimicrobial Wound SolutionFRO · Traditional Letus Corporation03/25/2026SE
K251999Promogran Prisma™ Collagen Matrix with ORC and SilverFRO · Traditional Solventum Germany GmbH03/13/2026SE

Questions and answers

When was LUOFUCON® Antimicrobial Wound Gel cleared by the FDA?

LUOFUCON® Antimicrobial Wound Gel (K252028) received a 510(k) decision of Substantially Equivalent on March 11, 2026, 254 days after the submission was received.

What is the product code of K252028?

The FDA product code is FRO – Dressing, Wound, Drug, a Unclassified device.