Cleared Traditional

Theracor

K253339 · Stimlabs, LLC · General & Plastic Surgery
Dec 2025
Decision
83d
Days
Risk

About This 510(k) Submission

K253339 is an FDA 510(k) clearance for the Theracor, a Wound Dressing With Animal-derived Material(s), submitted by Stimlabs, LLC (Roswell, US). The FDA issued a Cleared decision on December 22, 2025, 83 days after receiving the submission on September 30, 2025. This device falls under the General & Plastic Surgery review panel.

Submission Details

510(k) Number K253339 FDA.gov
FDA Decision Cleared SESE
Date Received September 30, 2025
Decision Date December 22, 2025
Days to Decision 83 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