AMIRIX IMAGING

FDA Device Registration & Listing · Newbury Park, CA, US · Registration 3032799939

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
3032799939
FEI Number
3032799939
Entity Name
AMIRIX IMAGING
City/State/Country
Newbury Park, CA, US
Establishment Address
1200 Lawrence Dr Ste 200, Newbury Park, CA 91320, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Amirix Imaging LLC (Owner Number: 10091332)
Owner / Operator Contact Address
1200 Lawrence Drive, Ste 200, Newbury Park, CA 91320, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

LM33-T

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ITY Assembly, Tube Housing, X-Ray, Diagnostic Radiology Class 1 892.1760 2024-08-27

Official Correspondent

Lars Aagaard

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Amirix Imaging LLC
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 3032799939. Last updated year: 2026. Please use registration number 3032799939 when referencing this establishment in official correspondence.
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