Cleared Traditional

MatriDerm pluS+ Bi-Layer

K250864 · Medskin Solutions Dr. Suwelack AG · General & Plastic Surgery
Dec 2025
Decision
273d
Days
Risk

About This 510(k) Submission

K250864 is an FDA 510(k) clearance for the MatriDerm pluS+ Bi-Layer, a Wound Dressing With Animal-derived Material(s), submitted by Medskin Solutions Dr. Suwelack AG (Billerbeck, DE). The FDA issued a Cleared decision on December 19, 2025, 273 days after receiving the submission on March 21, 2025. This device falls under the General & Plastic Surgery review panel.

Submission Details

510(k) Number K250864 FDA.gov
FDA Decision Cleared SESE
Date Received March 21, 2025
Decision Date December 19, 2025
Days to Decision 273 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