← Back to catalogue

Trigen

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
TRIGEN FDA UDI
Generic Name
Tibia intramedullary nail FDA UDI
Device Name
TRIGEN KNEE NAIL GOLD 10MM X 26CM RETROGRADE FEMUR/TIBIA MODES FDA UDI
Model / Reference
71633226 FDA UDI
Description
TRIGEN KNEE NAIL GOLD 10MM X 26CM RETROGRADE FEMUR/TIBIA MODES FDA UDI

Identifiers

Catalog Number
71633226 FDA UDI
Primary DI / UDI-DI
03596010425010 FDA UDI
510(k) Number
K210980 FDA UDI
K981529 FDA UDI
FDA Product Code
JDS FDA UDI
GMDN Term
Tibia 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: Tibia intramedullary nail

Trigen by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tibia intramedullary nail.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 3a503e21-cd98-4e88-9206-53c5e397a666 36 fields · synced Jun 8, 2026