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EzDebride EZ-001

by Mdm Wound Ventures Inc. 2 variants

EzDebride EZ-001 is a manual wound debridement tool (FDA Class I; FDA product code KDD, Kit, Surgical Instrument, Disposable) made by Mdm Wound Ventures Inc., listed in FDA GUDID since 31 May 2023 (UDI-DI 10860010005917), registry data as of 8 Nov 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 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10860010005917 UDI-DI Date31 May 2023ListedStatusListed 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  • Withdrawn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
EzDebride
Generic name
Manual wound debridement tool
Model / reference
EZ-001
Primary DI / UDI-DI
10860010005917
FDA product code
KDD
GMDN term
Manual wound debridement tool
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Wound debridement tool

Similar devices

Other devices filed under FDA product code KDD (Kit, Surgical Instrument, Disposable).

Other devices from Mdm Wound Ventures Inc.

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)