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VeriCyn Wound Wash VWW-2003

by Armis Biopharma, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850022135316 UDI-DI Date30 Jul 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
VeriCyn Wound Wash
Generic Name
Antimicrobial wound irrigation solution
Model / Reference
VWW-2003
Primary DI / UDI-DI
00850022135316
510(k) Number
FDA Product Code
FQH
GMDN Term
Antimicrobial wound irrigation solution
Device Class
Class II
Regulation Number
880.5475
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K220759)

Other devices from Armis Biopharma, Inc.

Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No