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Legion

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
Legion FDA UDI
Generic Name
Surgical instrument guard, reusable FDA UDI
Device Name
OVAL PATELLA PROTECTOR WITH SPIKES 29MM FDA UDI
Model / Reference
E0017032-1 FDA UDI
Description
OVAL PATELLA PROTECTOR WITH SPIKES 29MM FDA UDI

Identifiers

Catalog Number
E0017032-1 FDA UDI
Primary DI / UDI-DI
00885556788479 FDA UDI
510(k) Number
K121393 FDA UDI
FDA Product Code
HRY FDA UDI
GMDN Term
Surgical instrument guard, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3530 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical instrument guard, reusable

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

Similar devices

Also classified as Surgical instrument guard, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9428b190-e914-44c1-a287-19d636d43f21 36 fields · synced Jun 8, 2026