FDA 510(k)

InnovaMatrix®FD

K-Number: K241866 · 2024-07-26

ApplicantConvatec Triad Life Sciences, LLC

Decision Date2024-07-26

Product CodeKGN

DecisionSubstantially Equivalent

Device Summary

InnovaMatrix®FD is the device name listed in this FDA 510(k) record. The listed applicant is Convatec Triad Life Sciences, LLC. It received FDA 510(k) clearance on 2024-07-26 under 510(k) number K241866. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the InnovaMatrix®FD?

InnovaMatrix®FD is a medical device that received FDA 510(k) clearance on 2024-07-26. The listed applicant is Convatec Triad Life Sciences, LLC. The 510(k) number is K241866.

When did InnovaMatrix®FD receive FDA 510(k) clearance?

InnovaMatrix®FD received FDA 510(k) clearance on 2024-07-26, under 510(k) number K241866.

Who is the listed applicant for InnovaMatrix®FD?

The FDA 510(k) record lists Convatec Triad Life Sciences, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for InnovaMatrix®FD?

The FDA product code for InnovaMatrix®FD is KGN.

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.

K260596Collagen Wound PowderVentris Medical K260669Endoform Dermal TemplateAroa Biosurgery , Ltd.K253521ECMT-100 WMDEcm Therapeutics, Inc.K253204CatalyzeBioTissue Holdings, Inc.K254034Roosin Collagen PowderRoosin Medical Co., Ltd.K253974Roosin Collagen DressingRoosin Medical Co., Ltd.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.