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. It is manufactured by Sioxmed, LLC. The 510(k) number is K222189.
When was SiOxD Wound Matrix approved by the FDA?
SiOxD Wound Matrix received FDA 510(k) clearance on 2022-11-18, under approval number K222189.
What company makes SiOxD Wound Matrix?
SiOxD Wound Matrix is manufactured by Sioxmed, LLC.
What is the FDA product code for SiOxD Wound Matrix?
The FDA product code for SiOxD Wound Matrix is QSZ.
Related Clinical Trials
Other Devices by Sioxmed, LLC
Related Devices (Code: QSZ)
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.