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Integra®

FDA UDI

Class U (US FDA UDI)

by Integra Lifesciences Corp.

Identity

Trade Name
Integra® FDA UDI
Generic Name
Animal-derived wound matrix dressing FDA UDI
Device Name
Integra® Wound Matrix (Thin) FDA UDI
Model / Reference
58101T FDA UDI
Description
Integra® Wound Matrix (Thin) FDA UDI

Identifiers

Catalog Number
58101T FDA UDI
Primary DI / UDI-DI
10381780032434 FDA UDI
510(k) Number
K113104 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 — 10 Inch FDA UDI
Width — 8 Inch FDA UDI
Width — 20 Centimeter FDA UDI
Length — 25 Centimeter FDA UDI

Category: Animal-derived wound matrix dressing

Integra® by Integra Lifesciences Corp. — 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 76c9c231-33d7-412b-856b-be56ce37d7b1 38 fields · synced Jun 8, 2026