Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3044320625

FEI Number

3044320625

Entity Name

AIRICU INC.

City/State/Country

City of Industry, CA, US

Establishment Address

220 N California Ave Ste A, City of Industry, CA 91744, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198

Owner / Operator

AIRICU INC. (Owner Number: 10095528)

Owner / Operator Contact Address

220 N California Ave Ste A, City of Industry, CA 91744, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K251584

PMA Number

N/A

All Registered Proprietary Names

Medication Cup Air Flow Sensor Sensor Adapter Adult T-Piece Medical Mesh Nebulizer Medical Mesh Nebulizer AirICU Max+ ST

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
SFP	Ventilator-Compatible Nebulizer	Anesthesiology	Class 2	868.5630	2026-03-24

Official Correspondent

Jay Li

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

AIRICU INC.

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 3044320625. Last updated year: 2026. Please use registration number 3044320625 when referencing this establishment in official correspondence.