← Back to catalogue

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
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
D090101329290 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

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

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.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI b15bc529-4857-424d-81b8-3b562b852987 34 fields · synced Jun 9, 2026