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LinkBio Instrument 87-2003/03

by LinkBio Corp.

LinkBio Instrument 87-2003/03 is a Class I device made by LinkBio Corp., listed in FDA GUDID since 8 Jun 2026 (UDI-DI 00810022403457), 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 Number00810022403457 UDI-DI Date8 Jun 2026ListedStatusListed 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  • Withdrawn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
Orthopaedic prosthesis implantation positioning instrument, reusable
Model / reference
87-2003/03
Primary DI / UDI-DI
00810022403457
FDA product code
HWT
GMDN term
Orthopaedic prosthesis implantation positioning instrument, reusable
Device class
Class I
Regulation number
888.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

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)