NOMAD Pro 2

FDA UDI

Class II (US FDA UDI)

by Dental Imaging Technologies Corporation

Identity

Trade Name: NOMAD Pro 2 FDA UDI
Generic Name: Diagnostic x-ray system generator, hand-held FDA UDI
Device Name: X-Ray Tubehead, DEXIS Nomad Pro 2, GBL FDA UDI
Model / Reference: 1.013.2930 FDA UDI
Description: X-Ray Tubehead, DEXIS Nomad Pro 2, GBL FDA UDI

Identifiers

Primary DI / UDI-DI: D090101329300 FDA UDI
510(k) Number: K173319 FDA UDI
FDA Product Code: EHD FDA UDI
GMDN Term: Diagnostic x-ray system generator, hand-held FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 872.1800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Diagnostic x-ray system generator, hand-held

NOMAD Pro 2 by Dental Imaging Technologies Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Diagnostic x-ray system generator, hand-held.

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NOMAD™ handheld X-ray system — ARIBEX, INC. · Class II
NOMAD™ handheld X-ray system — ARIBEX, INC. · Class II
NOMAD Pro 2™ — ARIBEX, INC. · Class II
DTE — Guilin Woodpecker Medical Instrument Co., Ltd. · Class II
Packaged System, Kavo Nomad Pro2, US — ARIBEX, INC. · Class II

Cleared under the same submission

K173319 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Dental Imaging Technologies Corporation

Sources (1)

FDA UDI ed27f1d9-0e77-4f17-a949-cf8c93e65048 34 fields · synced Jun 9, 2026