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enforcement Primary ID: Z-1672-2015

LCS COMPLETE RPS Femoral Implants, various sizes and orientation. Knee prosthesis component for orthopedic surgery. (UDI Z-1672-2015)

Manufactured by DePuy Orthopaedics, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LCS COMPLETE RPS Femoral Implants, various sizes and orientation. Knee prosthesis component for orthopedic surgery. - Primary ID Z-1672-2015

Device Regulatory Overview

The LCS COMPLETE RPS Femoral Implants, various sizes and orientation. Knee prosthesis component for orthopedic surgery. (Model/Catalog Number: Unspecified) is a medical device manufactured by DePuy Orthopaedics, Inc.. This product is indexed under FDA Product Code / Category Classification All Lots. Catalog numbers: 129411010 129411020 129411030 129411040 129411050 129411060 129411070 129412010 129412020 129412030 129412040 129412050 129412060 129412070 129495040 129495050 129495060 129496040 129496050 129496060 within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 3 Event(s) Found

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Technical Specifications

Model Number
N/A
Device Name
LCS COMPLETE RPS Femoral Implants, various sizes and orientation. Knee prosthesis component for orthopedic surgery.
Database Sync Date
2026-08-09 10:06:38

Full Regulatory Attributes

🔒 Token Gated 
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of LCS COMPLETE RPS Femoral Implants, various sizes and orientation. Knee prosthesis component for orthopedic surgery.?

The registered manufacturer of record for LCS COMPLETE RPS Femoral Implants, various sizes and orientation. Knee prosthesis component for orthopedic surgery. is DePuy Orthopaedics, Inc..

What is the Primary UDI-DI identifier for LCS COMPLETE RPS Femoral Implants, various sizes and orientation. Knee prosthesis component for orthopedic surgery.?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Z-1672-2015.

What classification code is assigned to this device?

This device is registered under product classification code All Lots. Catalog numbers: 129411010 129411020 129411030 129411040 129411050 129411060 129411070 129412010 129412020 129412030 129412040 129412050 129412060 129412070 129495040 129495050 129495060 129496040 129496050 129496060.

Other Devices by DePuy Orthopaedics, Inc.

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