Tool · 510(k)

510(k) Predicate Finder

Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.

Product Code: KGN FDA unclassified

Wound Dressing With Animal-Derived Material(S)

Unknown

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Wound Dressing with Animal-Derived Material(s) is a dressing incorporating biological components sourced from animals, such as collagen or other extracellular matrix materials, used to cover wounds and support healing through biologically active mechanisms. This device is currently unclassified by the FDA, meaning it has not yet been placed into Class 1, 2, or 3 through the classification process, and a 510(k) submission has been required pending classification. The product code is KGN; no regulation number or medical specialty code has been assigned. This device is an implant.

510(k) Clearances

50+ matches
K Number
Device Name
GeniPhys Collymer Self-Assembling Scaffold
CollOvine™ Wound Dressing
DermiSphere Dermal Template
Bovine Dermis Collagen Dermal Matrix
BIOBRANE Temporary Wound Dressing; BIOBRANE Glove
Corplex P/ Theracor P/ Allacor P
ABCcolla® Collagen ADM Scaffold
Kerecis Parvus (50207)
InnovaMatrix®FD
MicroMatrix® UBM Particulate
Cytal® Wound Matrix; Cytal® Burn Matrix
LUOFUCON® Collagen Particles (Collagen Wound Dressing)
Miro3D Fibers Wound Matrix
ReyaGel (RG03 - MTP gel 3mL)
MiroDry Wound Matrix
Corplex P / Theracor P / Allacor P
MiroTract Wound Matrix
Comatryx OTC
Collagen Wound Dressing
SurgiAid® Collagen Wound Dressing
MicroMatrix® Flex
NovoGen Wound Matrix
FortiShield (Biosynthetic Wound Matrix)
Miro3D Wound Matrix
InnovaBurn
InnovaMatrix PD
LUOFUCON Collagen Wound Dressing
Miro3D Wound Matrix
PELNAC Meshed Bilayer Wound Matrix
PuraPly Micronized Wound Matrix (PuraPly MZ)
Kerecis Silicone
Fibrillar Collagen Wound Dressing
Geistlich Wound Matrix PLUS
PELNAC Wound Matrix
Cellusheet, Cellufil
INTEGRA Wound Matrix (Macro-Channels)
NeoMatriX Wound Matrix
InnovaMatrix FS
Myriad Particles
MatriDerm
InnovaMatrix
Symphony
KeraStat Cream
PELNAC Bilayer Wound Matrix
scaffolene CL100 Bioresorbable Collagen Matrix
Cytal Wound Matrix 3-Layer
MariGen Wound Extra
ProgenaMatrix
Geistlich Derma-Gide
NeoMatriX Wound Matrix

What is a Predicate Device?

A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.

Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.

Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.

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