Identity
- Trade Name
- LCS FDA UDI
- Generic Name
- Patella prosthesis trial FDA UDI
- Device Name
- LCS 3 PEG POLY PATELLA TRIAL WITH PEGS STD+ FDA UDI
- Model / Reference
- 2289-04-010 FDA UDI
- Description
- LCS 3 PEG POLY PATELLA TRIAL WITH PEGS STD+ FDA UDI
Identifiers
- Catalog Number
- 228904010 FDA UDI
- Primary DI / UDI-DI
- 10603295110590 FDA UDI
- FDA Product Code
- HWT FDA UDI
- GMDN Term
- Patella prosthesis trial FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4800 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Patella prosthesis trial
Lcs by Depuy Orthopaedics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Patella prosthesis trial.
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- Biomet® Series A™ — Biomet Orthopedics, Inc. · Class II
- JOURNEY — Smith & Nephew, Inc. · Class II
- Gender Solutions® Natural-Knee® — Zimmer, Inc. · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Depuy Orthopaedics, Inc.
Sources (1)
- FDA UDI 330235cb-7a5c-457f-92df-9494a8e73fa5 35 fields · synced Jun 8, 2026