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Duocentric® 50392

by Aston Medical

Duocentric® 50392 (30540040) is a Class II device made by Aston Medical, listed in FDA GUDID since 16 Sep 2015 (UDI-DI 03663703000868), 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 Number03663703000868 UDI-DI Date16 Sep 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  • Withdrawn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
Duocentric®
Generic name
Polyethylene reverse shoulder prosthesis cup
Model / Ref / Catalog
50392, 30540040
Primary DI / UDI-DI
03663703000868
FDA product code
KWS
GMDN term
Polyethylene reverse shoulder prosthesis cup
Device class
Class II
Regulation number
888.3660
GUDID distribution status
In Commercial Distribution

Related devices

Category: Polyethylene reverse shoulder prosthesis cup

Similar devices in this category

Other devices filed under Polyethylene reverse shoulder prosthesis cup.

Other devices from Aston Medical

See all devices from Aston Medical →

Properties

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