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Wound Matrix

FDA UDI

Class U (US FDA UDI)

by NovaBone Products, LLC

Identity

Trade Name
Wound Matrix FDA UDI
Generic Name
Animal-derived wound matrix dressing FDA UDI
Device Name
Collagen wound dressing FDA UDI
Model / Reference
WM0123 FDA UDI
Description
Collagen wound dressing FDA UDI

Identifiers

Catalog Number
WM0123 FDA UDI
Primary DI / UDI-DI
00813909012834 FDA UDI
510(k) Number
K220498 FDA UDI
FDA Product Code
KGN FDA UDI
GMDN Term
Animal-derived wound matrix dressing FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 3 Inch FDA UDI
Width — 2 Inch FDA UDI

Category: Animal-derived wound matrix dressing

Wound Matrix by NovaBone Products, LLC — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Animal-derived wound matrix dressing.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 298c28b6-f57e-48ea-aa5d-b2ecf63c2860 37 fields · synced Jun 9, 2026