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creos™

FDA UDI

Class III (US FDA UDI)

by Integra Lifesciences Corp.

Identity

Trade Name
creos™ FDA UDI
Generic Name
General oral wound dressing, animal-derived FDA UDI
Device Name
creos™ xenocote Absorbable Collagen Wound Dressing for Dental Surgery FDA UDI
Model / Reference
WD62201 FDA UDI
Description
creos™ xenocote Absorbable Collagen Wound Dressing for Dental Surgery FDA UDI

Identifiers

Catalog Number
WD62201 FDA UDI
Primary DI / UDI-DI
10381780490029 FDA UDI
FDA Product Code
LPG FDA UDI
GMDN Term
General oral wound dressing, animal-derived FDA UDI

Classification

Device Class
Class III 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

Category: General oral wound dressing, animal-derived

creos™ by Integra Lifesciences Corp. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General oral wound dressing, animal-derived.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0be49e0a-2a74-4394-9a70-310671034b7d 37 fields · synced May 29, 2026