Cleared Traditional

K251929 - SilverCeuticals® Antimicrobial Wound Gel

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Jun 2026
Decision
366d
Days
-
Risk

K251929 is an FDA 510(k) clearance for the SilverCeuticals® Antimicrobial Wound Gel. Classified as Dressing, Wound, Drug (product code FRO).

Submitted by Silverceuticals, Inc. (Lindon, US). The FDA issued a Cleared decision on June 24, 2026 after a review of 366 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the General & Plastic Surgery FDA review panel. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Elevated predicate reliance profile. This clearance follows a standard predicate-based equivalence path within the General & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.

View all Silverceuticals, Inc. devices

FDA 510(k) Submission Details - K251929

510(k) Number K251929 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 23, 2025
Decision Date June 24, 2026
Days to Decision 366 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
PCCP Authorized No
Regulatory Context
Review time vs. panel average
251d slower than avg
Panel avg: 115d · This submission: 366d
Pathway characteristics
Predicate-based equivalence.

FRO Device Classification - Class 0,

Product Code FRO Dressing, Wound, Drug
Device Class -

Regulatory Peers - FRO Dressing, Wound, Drug

All 606
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