← Back to catalogue

Oxinium

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
OXINIUM FDA UDI
Generic Name
Metallic femoral head prosthesis FDA UDI
Device Name
OXINIUM FEMORAL HEAD 10/12 22MM +0 EXTENSION FDA UDI
Model / Reference
71341905 FDA UDI
Description
OXINIUM FEMORAL HEAD 10/12 22MM +0 EXTENSION FDA UDI

Identifiers

Catalog Number
71341905 FDA UDI
Primary DI / UDI-DI
00885556112533 FDA UDI
510(k) Number
K110101 FDA UDI
FDA Product Code
LZO FDA UDI
GMDN Term
Metallic femoral head prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3353 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: Metallic femoral head prosthesis

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

Similar devices

Also classified as Metallic femoral head prosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI f90fb1c9-01f4-45d5-85b9-326fbc391e1e 36 fields · synced Jun 8, 2026