Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012114684

FEI Number

3012114684

Entity Name

AZTEC

City/State/Country

Lakeville, MN, US

Establishment Address

21455 Hamburg Ave, Lakeville, MN 55044, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Aztec (Owner Number: 10092277)

Owner / Operator Contact Address

21455 Hamburg Ave, Lakeville, MN 55044, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LXZ	Guard, Instrument	General, Plastic Surgery	Class 1	878.4800	2024-12-19

Official Correspondent

Keith Koecher

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Aztec

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 3012114684. Last updated year: 2026. Please use registration number 3012114684 when referencing this establishment in official correspondence.