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LinkBio Instrument 87-1401

by LinkBio Corp.

LinkBio Instrument 87-1401 is a Class I device made by LinkBio Corp., listed in FDA GUDID since 28 Mar 2023 (UDI-DI 00810022403020), 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 Number00810022403020 UDI-DI Date28 Mar 2023ListedStatusListed 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  • Withdrawn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
LinkBio Instrument
Generic name
Knee stem prosthesis trial
Model / reference
87-1401
Primary DI / UDI-DI
00810022403020
FDA product code
HWT
GMDN term
Knee stem prosthesis trial
Device class
Class I
Regulation number
888.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Knee stem prosthesis trial

Other devices from LinkBio Corp.

See all devices from LinkBio Corp. →

Properties

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