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creos™ WD62201

by Integra Lifesciences Corp.

creos™ WD62201 is a Class III device made by Integra Lifesciences Corp., listed in FDA GUDID since 28 Sep 2018 (UDI-DI 10381780490029), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10381780490029 UDI-DI Date28 Sep 2018ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
creos™
Generic name
General oral wound dressing, animal-derived
Model / Ref / Catalog
WD62201
Primary DI / UDI-DI
10381780490029
FDA product code
LPG
GMDN term
General oral wound dressing, animal-derived
Device class
Class III
GUDID distribution status
In Commercial Distribution

Related devices

Category: General oral wound dressing, animal-derived

Similar devices in this category

Other devices filed under General oral wound dressing, animal-derived.

Other devices from Integra Lifesciences Corp.

See all devices from Integra Lifesciences Corp. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)