Identity
- Trade Name
- LCS COMPLETE FDA UDI
- Generic Name
- Uncoated knee femur prosthesis, metallic FDA UDI
- Device Name
- LCS COMPLETE MODULAR FEMORAL CEMENTED SM LEFT FDA UDI
- Model / Reference
- 1294-42-010 FDA UDI
- Description
- LCS COMPLETE MODULAR FEMORAL CEMENTED SM LEFT FDA UDI
Identifiers
- Catalog Number
- 129442010 FDA UDI
- Primary DI / UDI-DI
- 10603295026136 FDA UDI
- FDA Product Code
- NJL FDA UDI
- GMDN Term
- Uncoated knee femur prosthesis, metallic FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Uncoated knee femur prosthesis, metallic
Lcs Complete by Depuy Orthopaedics, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Balance Knee Revision System — ORTHO DEVELOPMENT CORP. · Class II
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 III | Pending data |
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Manufacturer
- Manufacturer
- Depuy Orthopaedics, Inc.
Sources (1)
- FDA UDI 0567fa30-0293-4f28-9837-29e63c3fb4ee 35 fields · synced Jun 6, 2026