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Arthrex® AR-4515

by Arthrex, Inc.

Arthrex® AR-4515 is a Class I device made by Arthrex, Inc., listed in FDA GUDID since 3 May 2018 (UDI-DI 00888867033542), 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 Number00888867033542 UDI-DI Date3 May 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  • Withdrawn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
Suture trimmer
Model / Ref / Catalog
AR-4515
Primary DI / UDI-DI
00888867033542
FDA product code
MDM
GMDN term
Suture trimmer
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Suture trimmer

Similar devices

Also classified as Suture trimmer.

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)