Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008105001

FEI Number

3008105001

Entity Name

LUMADENT INC

City/State/Country

Reno, NV, US

Establishment Address

10437 Double R Blvd, Reno, NV 89521, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

LUMADENT INC. (Owner Number: 10038209)

Owner / Operator Contact Address

10437 Double R Blvd, Reno, NV 89521, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ProLUX airLUX uniLUX waveLUX

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KYT	Light, Examination, Medical, Battery Powered	General Hospital	Class 1	880.6350	2011-09-23

Official Correspondent

Don Ton

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

LUMADENT INC.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008105001. Last updated year: 2026. Please use registration number 3008105001 when referencing this establishment in official correspondence.