SiOxD Wound Matrix
K-Number: K222189 · 2022-11-18
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 2022-11-18. The listed applicant is Sioxmed, LLC. The 510(k) number is K222189.
When did SiOxD Wound Matrix receive FDA 510(k) clearance?
SiOxD Wound Matrix received FDA 510(k) clearance on 2022-11-18, under 510(k) number K222189.
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.