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FO NX Nail System

FDA UDI

Class I (US FDA UDI)

by Field Orthopaedics Pty Ltd

Identity

Trade Name
FO NX Nail System FDA UDI
Generic Name
Surgical depth gauge, reusable FDA UDI
Device Name
5.0 NX Depth Gauge 1/pkg FDA UDI
Model / Reference
APN000257 FDA UDI
Description
5.0 NX Depth Gauge 1/pkg FDA UDI

Identifiers

Catalog Number
NXDG-50/1 FDA UDI
Primary DI / UDI-DI
09353903009108 FDA UDI
FDA Product Code
HTJ FDA UDI
GMDN Term
Surgical depth gauge, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4300 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical depth gauge, reusable

FO NX Nail System by Field Orthopaedics Pty Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical depth gauge, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a66f4767-6dbd-4d1a-88bf-badf94d86769 34 fields · synced Jun 1, 2026