Skip to content

Promos 75005240

by Smith & Nephew, Inc.

Promos 75005240 is a Class I device made by Smith & Nephew, Inc., listed in FDA GUDID since 25 Nov 2015 (UDI-DI 07611996086973), 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 Number07611996086973 UDI-DI Date25 Nov 2015ListedStatusListed 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  • Withdrawn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
Promos
Generic name
Reverse shoulder cup prosthesis trial, reusable
Model / Ref / Catalog
75005240
Primary DI / UDI-DI
07611996086973
FDA product code
LXH
GMDN term
Reverse shoulder cup prosthesis trial, reusable
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Reverse shoulder cup prosthesis trial, reusable

Other devices from Smith & Nephew, Inc.

See all devices from Smith & Nephew, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)