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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
General internal orthopaedic fixation system implantation kit FDA UDI
Device Name
ENTRY REAMER FDA UDI
Model / Reference
1 FDA UDI
Description
ENTRY REAMER FDA UDI

Identifiers

Catalog Number
183270 FDA UDI
Primary DI / UDI-DI
18054242519072 FDA UDI
510(k) Number
K172699 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
General internal orthopaedic fixation system implantation kit 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

Category: General internal orthopaedic fixation system implantation kit

Agile Nail by Orthofix, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General internal orthopaedic fixation system implantation kit.

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 2d45e555-6dab-4786-b21e-e14dcdc52229 36 fields · synced May 30, 2026