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Arthrex® AR-1259

by Arthrex, Inc.

Arthrex® AR-1259 is a Class I device made by Arthrex, Inc., listed in FDA GUDID since 29 Apr 2018 (UDI-DI 00888867006645), 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 Number00888867006645 UDI-DI Date29 Apr 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  • Withdrawn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
Suturing unit, single-use
Model / Ref / Catalog
AR-1259
Primary DI / UDI-DI
00888867006645
FDA product code
MDM
GMDN term
Suturing unit, single-use
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Suturing unit, single-use

Similar devices in this category

Other devices filed under Suturing unit, single-use.

Other devices from Arthrex, Inc.

See all devices from Arthrex, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)