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Arthrex® AR-9502-33ARCA

by Arthrex, Inc.

Arthrex® AR-9502-33ARCA is a Class II device made by Arthrex, Inc., listed in FDA GUDID since 29 Mar 2024 (UDI-DI 00888867406452), 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 Number00888867406452 UDI-DI Date29 Mar 2024ListedStatusListed 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  • Withdrawn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
Shoulder reverse/standard adaptor prosthesis
Model / Ref / Catalog
AR-9502-33ARCA
Primary DI / UDI-DI
00888867406452
FDA product code
HSD
GMDN term
Shoulder reverse/standard adaptor prosthesis
Device class
Class II
Regulation number
888.3690
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

Related devices

Category: Shoulder reverse/standard adaptor prosthesis

Similar devices

Other devices filed under FDA product code HSD (PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED).

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)