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Arthrex® AR-7290

by Arthrex, Inc.

Arthrex® AR-7290 is a Class II device made by Arthrex, Inc., listed in FDA GUDID since 13 Jun 2025 (UDI-DI 00888867301986), 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 Number00888867301986 UDI-DI Date13 Jun 2025ListedStatusListed 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  • Withdrawn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
Polyolefin/fluoropolymer suture, multifilament
Model / Ref / Catalog
AR-7290
Primary DI / UDI-DI
00888867301986
FDA product code
OWX, FTL
GMDN term
Polyolefin/fluoropolymer suture, multifilament
Device class
Class II
Regulation number
878.3300
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe

Related devices

Category: Soft-tissue/mesh anchor, bioabsorbable

Similar devices

Other devices filed under FDA product code OWX (Mesh, surgical, non-absorbable, orthopaedics, reinforcement of tendon).

Other devices from Arthrex, Inc.

See all devices from Arthrex, Inc. →

Properties

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