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FDA 510(k)

InnovaMatrix PD

K-Number: K211902 · 2022-09-28

ApplicantTriad Life Sciences, Inc.
Decision Date2022-09-28
Product CodeKGN
DecisionSubstantially Equivalent

Device Summary

InnovaMatrix PD is the device name listed in this FDA 510(k) record. The listed applicant is Triad Life Sciences, Inc.. It received FDA 510(k) clearance on 2022-09-28 under 510(k) number K211902. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the InnovaMatrix PD?

InnovaMatrix PD is a medical device that received FDA 510(k) clearance on 2022-09-28. The listed applicant is Triad Life Sciences, Inc.. The 510(k) number is K211902.

When did InnovaMatrix PD receive FDA 510(k) clearance?

InnovaMatrix PD received FDA 510(k) clearance on 2022-09-28, under 510(k) number K211902.

Who is the listed applicant for InnovaMatrix PD?

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

What is the FDA product code for InnovaMatrix PD?

The FDA product code for InnovaMatrix PD is KGN.

Other records listing Triad Life Sciences, Inc. 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.

K213716InnovaBurnK210580InnovaMatrix FSK193552InnovaMatrix

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 MedicalK260669Endoform 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.

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