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Duocentric® 43014STER

by Aston Medical

Duocentric® 43014STER (76042041) is a Class II device made by Aston Medical, listed in FDA GUDID since 16 Sep 2015 (UDI-DI 03663703001049), 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 Number03663703001049 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  • Withdrawn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
Shoulder prosthesis screw
Model / Ref / Catalog
43014STER, 76042041
Primary DI / UDI-DI
03663703001049
FDA product code
KWS
GMDN term
Shoulder prosthesis screw
Device class
Class II
Regulation number
888.3660
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 4.2 Millimeter
Length — 20 Millimeter

Related devices

Category: Shoulder prosthesis screw

Similar devices in this category

Other devices filed under Shoulder prosthesis screw.

Other devices from Aston Medical

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)