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Agile Nail

FDA UDI

Class II (US FDA UDI)

by Orthofix, Inc.

Identity

Trade Name
AGILE NAIL FDA UDI
Generic Name
Femur intramedullary nail FDA UDI
Device Name
AGILE NAIL TI NAIL RIGHT L280MM D7MM STERILE FDA UDI
Model / Reference
1 FDA UDI
Description
AGILE NAIL TI NAIL RIGHT L280MM D7MM STERILE FDA UDI

Identifiers

Catalog Number
99-T837280R FDA UDI
Primary DI / UDI-DI
18054242519447 FDA UDI
510(k) Number
K172699 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Femur intramedullary nail FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 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

Yes

FDA UDI

Dimensions & Sizes

Size
Width — 95 Millimeter FDA UDI

Category: Femur intramedullary nail

Agile Nail by Orthofix, 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

Manufacturer
Orthofix, Inc.

Sources (1)

  • FDA UDI a82f238f-5115-488f-a54b-91c4f1385702 37 fields · synced May 30, 2026