SiOxD® Wound Matrix
K-Number: K241660 · 2024-07-05
Device Summary
Frequently Asked Questions
What is the SiOxD® Wound Matrix?
SiOxD® Wound Matrix is a medical device that received FDA 510(k) clearance on 2024-07-05. The listed applicant is Sioxmed, LLC. The 510(k) number is K241660.
When did SiOxD® Wound Matrix receive FDA 510(k) clearance?
SiOxD® Wound Matrix received FDA 510(k) clearance on 2024-07-05, under 510(k) number K241660.
Who is the listed applicant for SiOxD® Wound Matrix?
The FDA 510(k) record lists Sioxmed, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SiOxD® Wound Matrix?
The FDA product code for SiOxD® Wound Matrix is QSZ.
Other records listing Sioxmed, LLC 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: QSZ)
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.