Identity
- Trade Name
- TITAN™ FDA UDI
- Generic Name
- Shoulder glenoid fossa prosthesis, prefabricated FDA UDI
- Device Name
- The Fin-Lock Glenoid implant is part of the Titan Modular Shoulder System. It is an anchor peg that is used in patients with severely painful and/or disabled joint, fracture-dislocations, and other difficult clinical problems where shoulder arthrodesis or resection arthroplasty are not acceptable. The glenoid component is intended for cemented use only. FDA UDI
- Model / Reference
- GLN-0926-030-03A FDA UDI
- Description
- The Fin-Lock Glenoid implant is part of the Titan Modular Shoulder System. It is an anchor peg that is used in patients with severely painful and/or disabled joint, fracture-dislocations, and other difficult clinical problems where shoulder arthrodesis or resection arthroplasty are not acceptable. The glenoid component is intended for cemented use only. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10381780258704 FDA UDI
- 510(k) Number
- K152047 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™ by Ascension Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Shoulder glenoid fossa prosthesis, prefabricated.
- PRIMA TT Glenoid — Limacorporate · Class II
- AEQUALIS REVERSED II — TORNIER, INC. · Class II
- INHANCE — DEPUY (IRELAND) · Class II
- Equinoxe — Exactech, Inc. · Class II
- Full Wedge Lateralized and Augmented Baseplates — FX SOLUTIONS · Class II
- SMR System — Limacorporate · Class II
- SMR Metal Back — Limacorporate · Class II
- AEQUALIS™ PerFORM — TORNIER, INC. · Class II
Cleared under the same submission
K152047 also covers:
- 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.
- 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
- Ascension Orthopedics, Inc.
Sources (1)
- FDA UDI 7379f211-f1bf-488e-9814-7a16821f13a9 37 fields · synced Jun 1, 2026