Titan Modular Shoulder System 2.5

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name: Titan Modular Shoulder System 2.5 FDA UDI
Generic Name: Shoulder glenoid fossa prosthesis trial FDA UDI
Device Name: GLENOID SIZER SMALL FDA UDI
Model / Reference: SZR-0920-052-001 FDA UDI
Description: GLENOID SIZER SMALL FDA UDI

Identifiers

Catalog Number: SZR-0920-052-001 FDA UDI
Primary DI / UDI-DI: 00885556862216 FDA UDI
FDA Product Code: HWT FDA UDI
GMDN Term: Shoulder glenoid fossa prosthesis trial FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.4800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

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: Shoulder glenoid fossa prosthesis trial

Titan Modular Shoulder System 2.5 by Smith & Nephew, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Shoulder glenoid fossa prosthesis trial.

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REUNION — Stryker Corp. · Class I
SMR Shoulder — Limacorporate · Class II
DJO SURGICAL — ENCORE MEDICAL, L.P. · Class I
REUNION — Stryker Corp. · Class I

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 7aa85eab-f933-414b-9f0e-c93041fcf98e 35 fields · synced Jun 6, 2026