Unite Biomatrix

FDA 510(k) K071425 · Pegasus Biologics, Inc.

Substantially Equivalent

510(k) numberK071425

Submission

Device name
Unite Biomatrix
Applicant
Pegasus Biologics, Inc.
Irvine, CA, US
Received
May 23, 2007
Decision date
June 20, 2007
Decision
Substantially Equivalent (SESE)
Type
Special 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

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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
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K254034Roosin Collagen PowderKGN · Traditional Roosin Medical Co., Ltd.06/03/2026SE
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

More from Geistlich Pharma AG

510(k)DeviceDecision
K090288Orthadapt PRFTL · Traditional 05/05/2009SE
K071065Orthadapt BioimplantFTM · Special 05/04/2007SE
K061494Dermadapt Wound DressingKGN · Traditional 09/21/2006SE
K043388Pegasus Biologics Orthadapt Surgical MeshFTM · Traditional 08/05/2005SE

Questions and answers

When was Unite Biomatrix cleared by the FDA?

Unite Biomatrix (K071425) received a 510(k) decision of Substantially Equivalent on June 20, 2007, 28 days after the submission was received.

What is the product code of K071425?

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