Identity
- Trade Name
- Titan Modular Shoulder System 2.5 FDA UDI
- Generic Name
- Shoulder glenoid fossa prosthesis, prefabricated FDA UDI
- Device Name
- FIN-LOCK GLENOID. XS FDA UDI
- Model / Reference
- GLN-0926-030-00A FDA UDI
- Description
- FIN-LOCK GLENOID. XS FDA UDI
Identifiers
- Catalog Number
- GLN-0926-030-00A FDA UDI
- Primary DI / UDI-DI
- 00885556860304 FDA UDI
- FDA Product Code
- KWS FDA UDI
- GMDN Term
- Shoulder glenoid fossa prosthesis, prefabricated 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
Category: Shoulder glenoid fossa prosthesis, prefabricated
Titan Modular Shoulder System 2.5 by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Shoulder glenoid fossa prosthesis, prefabricated.
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Cleared under the same submission
K152047 also covers:
- TITAN™ — Ascension Orthopedics, Inc.
- TITAN™ — Ascension Orthopedics, Inc.
- TITAN™ — Ascension Orthopedics, Inc.
- TITAN™ — Ascension Orthopedics, Inc.
- Titan Modular Shoulder System 2.5 — Smith & Nephew, Inc.
- Titan Modular Shoulder System 2.5 — Smith & Nephew, Inc.
- Titan Modular Shoulder System 2.5 — Smith & Nephew, Inc.
K213827 also covers:
- Katalyst Biopolar Radial Head System — Smith & Nephew, Inc.
- Katalyst Bipolar Radial Head System — Smith & Nephew, Inc.
- Modular Radial Head (MRH) System — Smith & Nephew, Inc.
- Modular Radial Head (MRH) System — Smith & Nephew, Inc.
- Modular Radial Head (MRH) System — Smith & Nephew, Inc.
- Titan Humeral Resurfacing Arthroplasty — Smith & Nephew, Inc.
- Titan Humeral Resurfacing Arthroplasty — Smith & Nephew, Inc.
- Titan Modular Shoulder System — Smith & Nephew, Inc.
- Titan Modular Shoulder System — Smith & Nephew, Inc.
- Titan Modular Shoulder System 2.5 — Smith & Nephew, Inc.
- Titan Modular Shoulder System 2.5 — Smith & Nephew, Inc.
- Titan Modular Shoulder System 2.5 — Smith & Nephew, Inc.
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 II | Pending data |
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Manufacturer
- Manufacturer
- Smith & Nephew, Inc.
Sources (1)
- FDA UDI 140f417c-175c-489c-a620-4d96e8839e77 36 fields · synced Jun 8, 2026