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Kirschner wire 290.25.280

by Zimmer, Inc.

Kirschner wire 290.25.280 is a Class I device made by Zimmer, Inc., listed in FDA GUDID since 5 Feb 2021 (UDI-DI 00889024394995), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00889024394995 UDI-DI Date5 Feb 2021ListedStatusListed 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  • Withdrawn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
Kirschner wire
Generic name
Internal orthopaedic fixation system, cerclage wire/cable, non-sterile
Model / Ref / Catalog
290.25.280
Primary DI / UDI-DI
00889024394995
FDA product code
FZX
GMDN term
Internal orthopaedic fixation system, cerclage wire/cable, non-sterile
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Internal orthopaedic fixation system, cerclage wire/cable, non-sterile

Other devices from Zimmer, Inc.

See all devices from Zimmer, Inc. →

Properties

  • Sterilise before use
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (9, all answered No)