Cleared Traditional

CollOvine? Wound Powder

K253140 · Ovigenex, LLC · General & Plastic Surgery
Feb 2026
Decision
138d
Days
Risk

About This 510(k) Submission

K253140 is an FDA 510(k) clearance for the CollOvine? Wound Powder, a Wound Dressing With Animal-derived Material(s), submitted by Ovigenex, LLC (Dominguez Hills, US). The FDA issued a Cleared decision on February 10, 2026, 138 days after receiving the submission on September 25, 2025. This device falls under the General & Plastic Surgery review panel.

Submission Details

510(k) Number K253140 FDA.gov
FDA Decision Cleared SESE
Date Received September 25, 2025
Decision Date February 10, 2026
Days to Decision 138 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code KGN — Wound Dressing With Animal-derived Material(s)
Device Class