Roosin Collagen Powder

FDA 510(k) K254034 · Roosin Medical Co., Ltd.

Substantially Equivalent

510(k) numberK254034

Submission

Device name
Roosin Collagen Powder
Applicant
Roosin Medical Co., Ltd.
Taizhou, CN
Received
December 16, 2025
Decision date
June 3, 2026
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KGN – Wound Dressing With Animal-Derived Material(S)
Device class
Unclassified
Implant
Yes

Other 510(k)s with product code KGN

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K260652ColActive PlusKGN · Traditional Covalon Technologies, Ltd.09/09/2026SE
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K260596Collagen Wound PowderKGN · Traditional Ventris Medical07/02/2026SE
K260669Endoform Dermal TemplateKGN · Traditional Aroa Biosurgery , Ltd.06/24/2026SE
K253521ECMT-100 WMDKGN · Traditional Ecm Therapeutics, Inc.06/18/2026SE
K253204CatalyzeKGN · Traditional BioTissue Holdings, Inc.06/05/2026SE
K253974Roosin Collagen DressingKGN · Traditional Roosin Medical Co., Ltd.06/03/2026SE
K261224MatriDermKGN · Special Medskin Solutions Dr. Suwelack AG05/14/2026SE
K260532Derma-GideKGN · Special Geistlich Pharma AG03/19/2026SE
K260218LacertaMatrixKGN · Special Lacerta Life Sciences02/19/2026SE

More from Lacerta Life Sciences

510(k)DeviceDecision
K253974Roosin Collagen DressingKGN · Traditional 06/03/2026SE
K231088Copper Foam Dressing (Prescription and OTC)FRO · Traditional 01/11/2024SE
K230190Polyver Silver Alginate Dressing (Prescription and OTC)FRO · Traditional 11/17/2023SE
K181478Roosin Xeroform Petrolatum DressingFRO · Traditional 09/13/2019SE

Questions and answers

When was Roosin Collagen Powder cleared by the FDA?

Roosin Collagen Powder (K254034) received a 510(k) decision of Substantially Equivalent on June 3, 2026, 169 days after the submission was received.

What is the product code of K254034?

The FDA product code is KGN – Wound Dressing With Animal-Derived Material(S), a Unclassified device.