Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2032792

FEI Number

3004129983

Entity Name

Q.T.I. CORP.

City/State/Country

Lake Havasu City, AZ, US

Establishment Address

1990 McCulloch Blvd. N Ste. 197, Lake Havasu City, AZ 86403, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Q.T.I. CORP. (Owner Number: 9057629)

Owner / Operator Contact Address

1990 McCulloch Blvd. N STE 197, Lake Havasu City, AZ 86403, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Skintestor OMNI

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LDH	N/A	N/A	Class N/A	N/A	2007-11-21

Official Correspondent

ALLAN TISO

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Q.T.I. CORP.

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 2032792. Last updated year: 2026. Please use registration number 2032792 when referencing this establishment in official correspondence.