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Titan™

FDA UDI

Class II (US FDA UDI)

by Ascension Orthopedics, Inc.

Identity

Trade Name
Titan™ FDA UDI
Generic Name
Uncoated shoulder humeral stem prosthesis FDA UDI
Device Name
Total Shoulder System Cemented Long Stem, 08 x 125mm FDA UDI
Model / Reference
S95002508125 FDA UDI
Description
Total Shoulder System Cemented Long Stem, 08 x 125mm FDA UDI

Identifiers

Catalog Number
STEM-0950-025-08125 FDA UDI
Primary DI / UDI-DI
10381780364139 FDA UDI
510(k) Number
K142413 FDA UDI
FDA Product Code
KWS FDA UDI
GMDN Term
Uncoated shoulder humeral stem prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3660 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

Dimensions & Sizes

Size
Outer Diameter — 8 Millimeter FDA UDI
Length — 125 Millimeter FDA UDI

Category: Uncoated shoulder humeral stem prosthesis

Titan™ by Ascension Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Uncoated shoulder humeral stem prosthesis.

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 e0acfff0-0cc2-482e-8c2d-e0b2c31b829b 39 fields · synced May 30, 2026