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KaVo NOMAD Pro 2

FDA UDI

Class II (US FDA UDI)

by Dental Imaging Technologies Corporation

Identity

Trade Name
KaVo NOMAD Pro 2 FDA UDI
Generic Name
Diagnostic x-ray system generator, hand-held FDA UDI
Device Name
KaVo NOMAD Pro 2, US FDA UDI
Model / Reference
1.013.2929 FDA UDI
Description
KaVo NOMAD Pro 2, US FDA UDI

Identifiers

Primary DI / UDI-DI
EKAV101329290 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
Not 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

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

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

Cleared under the same submission

K173319 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dental Imaging Technologies Corporation

Sources (1)

  • FDA UDI 259d1a8e-04be-4a37-a262-d046b2de039d 35 fields · synced Jun 9, 2026