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Arthrex AR-8941-12

by Provision

Arthrex AR-8941-12 is a Class I device made by Provision, listed in FDA GUDID since 17 May 2023 (UDI-DI B504OMAR8941120), 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 NumberB504OMAR8941120 UDI-DI Date17 May 2023ListedStatusListed GUDID: in commercial distribution

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  • Withdrawn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
Drilling power tool attachment, basic
Model / reference
AR-8941-12
Primary DI / UDI-DI
B504OMAR8941120
FDA product code
LXH
GMDN term
Drilling power tool attachment, basic
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution

Related devices

Category: Drilling power tool attachment, basic

Similar devices

Also classified as Drilling power tool attachment, basic.

Similar devices in this category

Other devices filed under Drilling power tool attachment, basic.

Other devices from Provision

See all devices from Provision →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)