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Arthrex® AR-4156KB

by Arthrex, Inc.

Arthrex AR-4156KB is a wire/ligature passer (FDA Class I; FDA product code MDM, Instrument, Manual, Surgical, General Use) made by Arthrex, Inc., listed in FDA GUDID since 20 Jun 2018 (UDI-DI 00888867032866), 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 Number00888867032866 UDI-DI Date20 Jun 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  • Withdrawn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
Arthrex®
Generic name
Wire/ligature passer, single-use
Model / Ref / Catalog
AR-4156KB
Primary DI / UDI-DI
00888867032866
FDA product code
MDM
GMDN term
Wire/ligature passer, single-use
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Wire/ligature passer, single-use

Other devices from Arthrex, Inc.

See all devices from Arthrex, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)