ELITechGroup Inc., Tucson

FDA Device Registration & Listing · Tucson, AZ, US · Registration 3044320359

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3044320359
FEI Number
3044320359
Entity Name
ELITechGroup Inc., Tucson
City/State/Country
Tucson, AZ, US
Establishment Address
3950 S. Country Club Rd., Suite #470, L, Tucson, AZ 85714, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
ELITechGroup Inc. (Owner Number: 1717966)
Owner / Operator Contact Address
370 West 1700 South, Logan, UT 84321, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Bruker Arc System Bruker Arc Blood Culture Kit

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QNJ Mass Spectrometry, Microorganism Identification, Blood Culture Microbiology Class 2 866.3378 2026-03-20

Official Correspondent

Roberto Ortiz

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ELITechGroup Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3011461582 ELITechGroup S.p.A. Torino Piedmont, IT
3003540236 ELITechGroup MDX LLC. Bothell, WA, US
3006091463 ELITechGroup MICROBIO SIGNES Var, FR
1717966 ELITechGroup Inc LOGAN, UT, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3044320359. Last updated year: 2026. Please use registration number 3044320359 when referencing this establishment in official correspondence.
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