Identity
- Trade Name
- TRIGEN FDA UDI
- Generic Name
- Femur intramedullary nail FDA UDI
- Device Name
- TRIGEN INTERTAN 10MM X 42CM 125DEGREE LEFT FDA UDI
- Model / Reference
- 71675229 FDA UDI
- Description
- TRIGEN INTERTAN 10MM X 42CM 125DEGREE LEFT FDA UDI
Identifiers
- Catalog Number
- 71675229 FDA UDI
- Primary DI / UDI-DI
- 03596010572271 FDA UDI
- 510(k) Number
- K040212 FDA UDI
- FDA Product Code
- JDS FDA UDI
- GMDN Term
- Femur intramedullary nail FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3030 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: Femur intramedullary nail
Trigen by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Femur intramedullary nail.
- GAMMA — Stryker Corp. · Class II
- A.R.T.™FEMORAL NAIL — Biomet Orthopedics, Inc. · Class II
- T2 ALPHA — Stryker Corp. · Class II
- PRECICE® Bone Transport System — NuVasive Specialized Orthopedics, Inc. · Class II
- T2 — Stryker Corp. · Class II
- 130° Ga-mma Nail — Auxein Medical Private Limited · Class II
- ARIX Femur Nail System — Jeil Medical Corporation · Class II
- GAMMA — Stryker Corp. · Class II
Cleared under the same submission
K040212 also covers:
- INTERTAN — Smith & Nephew, Inc.
- INTERTAN — Smith & Nephew, Inc.
- INTERTAN — Smith & Nephew, Inc.
- TRIGEN — Smith & Nephew, Inc.
- TRIGEN — Smith & Nephew, Inc.
- TRIGEN — Smith & Nephew, Inc.
- TRIGEN — Smith & Nephew, Inc.
- TRIGEN — Smith & Nephew, Inc.
- TRIGEN — Smith & Nephew, Inc.
- TRIGEN — Smith & Nephew, Inc.
- TRIGEN — Smith & Nephew, Inc.
- TRIGEN — 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 b55b1af0-a4c1-42bb-8b28-b3f0eba667c9 36 fields · synced Jun 8, 2026