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ODI Talon™ Intramedullary Hip Nail

FDA UDI

Class II (US FDA UDI)

by Orthopedic Designs North America, Inc.

Identity

Trade Name
ODI Talon™ Intramedullary Hip Nail FDA UDI
Generic Name
Femur intramedullary nail FDA UDI
Device Name
Proximal Femoral Nail, 125 degree - 210mm (11mm Distal Diameter) FDA UDI
Model / Reference
THN125210 FDA UDI
Description
Proximal Femoral Nail, 125 degree - 210mm (11mm Distal Diameter) FDA UDI

Identifiers

Primary DI / UDI-DI
B058THN1252101 FDA UDI
510(k) Number
K014189 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

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 11 Millimeter FDA UDI
Length — 210 Millimeter FDA UDI
Angle — 125 degree FDA UDI

Category: Femur intramedullary nail

ODI Talon™ Intramedullary Hip Nail by Orthopedic Designs North America, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Femur intramedullary nail.

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 1fd5c07d-aac9-4775-91fc-c3a4a208059c 36 fields · synced Jun 6, 2026