Legion

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name: LEGION FDA UDI
Generic Name: Polyethylene patella prosthesis FDA UDI
Device Name: LEGION PATELLA PREP KIT FDA UDI
Model / Reference: 71443131KT FDA UDI
Description: LEGION PATELLA PREP KIT FDA UDI

Identifiers

Catalog Number: 71443131KT FDA UDI
Primary DI / UDI-DI: 00885556534533 FDA UDI
FDA Product Code: LXH FDA UDI
GMDN Term: Polyethylene patella prosthesis FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.4540 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Polyethylene patella prosthesis

Legion by Smith & Nephew, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Polyethylene patella prosthesis.

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S-ROM NOILES — DEPUY (IRELAND) · Class II
LOSPA Total Knee System — Corentec Co., Ltd · Class II
ADVANCE® — MicroPort Orthopedics Inc. · Class II
Unity Total Knee System — CORIN LTD · Class II
Proven Gen-Flex PS Knee System — GLOBUS MEDICAL, INC. · 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 I	Pending data

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Manufacturer

Manufacturer: Smith & Nephew, Inc.

Sources (1)

FDA UDI 7af86a6c-f5b5-4a93-8572-31a2b2667b97 35 fields · synced Jun 8, 2026