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Lcs Complete 2294-16-115

by Depuy Orthopaedics, Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Overview

The LCS Complete RPS INSERT TRIAL SM 15mm is a reusable knee tibia prosthesis trial designed for unicompartmental knee replacement surgery or total knee arthroplasty (TKA). This device is made of metal or polymer material and features graduated sizes, including tibial base plate trials, tibial spacer trials, and guide pin trials. It is typically sterilized with Moist Heat or Steam Sterilization and has an expiration date, making it a valuable tool for medical professionals.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10603295111795 UDI-DI Date24 Sep 2018ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Lcs Complete
Generic Name
Knee tibia prosthesis trial, reusable
Model / Ref / Catalog
2294-16-115, 229416115
Primary DI / UDI-DI
10603295111795
FDA Product Code
HWT
GMDN Term
Knee tibia prosthesis trial, reusable
Device Class
Class I
Regulation Number
888.4800
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

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Properties

  • Premarket Exempt
  • Lot / Batch Number

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No