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Titan Modular Shoulder System 2.5

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
Titan Modular Shoulder System 2.5 FDA UDI
Generic Name
Surgical soft-tissue manipulation forceps, alligator, reusable FDA UDI
Device Name
TSS CEMENTED STEM SZ. 14 FDA UDI
Model / Reference
STEM-0950-025-14 FDA UDI
Description
TSS CEMENTED STEM SZ. 14 FDA UDI

Identifiers

Catalog Number
STEM-0950-025-14 FDA UDI
Primary DI / UDI-DI
00885556837757 FDA UDI
510(k) Number
K100448 FDA UDI
K112438 FDA UDI
K142413 FDA UDI
K213827 FDA UDI
FDA Product Code
HSD FDA UDI
KWS FDA UDI
GMDN Term
Surgical soft-tissue manipulation forceps, alligator, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3690 FDA UDI
888.3660 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical soft-tissue manipulation forceps, alligator, reusable

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

Similar devices

Also classified as Surgical soft-tissue manipulation forceps, alligator, 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 c7e20621-2540-41c5-ad3c-89ed0022800f 36 fields · synced Jun 8, 2026