MatriDerm
K-Number: K261224 · 2026-05-14
ApplicantMedskin Solutions Dr. Suwelack AG
Decision Date2026-05-14
Product CodeKGN
DecisionSubstantially Equivalent
Device Summary
MatriDerm is a medical device manufactured by Medskin Solutions Dr. Suwelack AG. It received FDA 510(k) clearance on 2026-05-14 under approval number K261224. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the MatriDerm?
MatriDerm is a medical device that received FDA 510(k) clearance on 2026-05-14. It is manufactured by Medskin Solutions Dr. Suwelack AG. The 510(k) number is K261224.
When was MatriDerm approved by the FDA?
MatriDerm received FDA 510(k) clearance on 2026-05-14, under approval number K261224.
What company makes MatriDerm?
MatriDerm is manufactured by Medskin Solutions Dr. Suwelack AG.
What is the FDA product code for MatriDerm?
The FDA product code for MatriDerm is KGN.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.