MatriDerm
K-Number: K261224 · 2026-05-14
Device Summary
Frequently Asked Questions
What is the MatriDerm?
MatriDerm is a medical device that received FDA 510(k) clearance on 2026-05-14. The listed applicant is Medskin Solutions Dr. Suwelack AG. The 510(k) number is K261224.
When did MatriDerm receive FDA 510(k) clearance?
MatriDerm received FDA 510(k) clearance on 2026-05-14, under 510(k) number K261224.
Who is the listed applicant for MatriDerm?
The FDA 510(k) record lists Medskin Solutions Dr. Suwelack AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MatriDerm?
The FDA product code for MatriDerm is KGN.
Other records listing Medskin Solutions Dr. Suwelack AG as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: KGN)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.