AMENICHI CONSULTING, LLC

FDA Device Registration & Listing · Chicago, IL, US · Registration 3019716369

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
3019716369
FEI Number
3019716369
Entity Name
AMENICHI CONSULTING, LLC
City/State/Country
Chicago, IL, US
Establishment Address
222 Merchandise Mart Plz Ste 228, Chicago, IL 60654, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198
Owner / Operator
Amenichi Consulting, LLC (Owner Number: 10082235)
Owner / Operator Contact Address
222 Merchandise Mart Plz Suite 1230, Chicago, IL 60654, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Peribeam

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DXZ Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene Cardiovascular Class 2 870.3470 2025-11-19

Official Correspondent

Keiji Asada

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Amenichi Consulting, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3019716369. Last updated year: 2026. Please use registration number 3019716369 when referencing this establishment in official correspondence.
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