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CORE Shoulder System 87-9138

by LinkBio Corp.

CORE Shoulder System 87-9138 is a Class I device made by LinkBio Corp., listed in FDA GUDID since 4 Jun 2025 (UDI-DI 00810022403112), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810022403112 UDI-DI Date4 Jun 2025ListedStatusListed 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  • Withdrawn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
CORE Shoulder System
Generic name
Surgical tray stand
Model / reference
87-9138
Primary DI / UDI-DI
00810022403112
FDA product code
FOX
GMDN term
Surgical tray stand
Device class
Class I
Regulation number
880.6990
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical tray stand

Similar devices

Other devices filed under FDA product code FOX (Stand, Infusion).

Other devices from LinkBio Corp.

See all devices from LinkBio Corp. →

Properties

  • Prescription use
  • Premarket exempt
Other properties (13, all answered No)