AQ THERAPEUTICS, INC.

FDA Device Registration & Listing · Irvine, CA, US · Registration 3023138850

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
3023138850
FEI Number
3023138850
Entity Name
AQ THERAPEUTICS, INC.
City/State/Country
Irvine, CA, US
Establishment Address
340 Goddard, Irvine, CA 92618, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
AQ Therapeutics, Inc. (Owner Number: 10085531)
Owner / Operator Contact Address
340 Goddard, Irvine, CA 92618, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

AQ Therapeutics Micro Adipose Processing System AQ Therapeutics Micro Adipose Processing System (MAPS) Kit AQ Therapeutics MAPS Kit

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GEA Cannula, Surgical, General & Plastic Surgery General, Plastic Surgery Class 1 878.4800 2022-06-29

Official Correspondent

Beverly Rattu

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K863293 Lifestream Int'L, Inc. DISPOSABLE SUCTION CANNULA NO. 902008-000 1986-09-09

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3023138850. Last updated year: 2026. Please use registration number 3023138850 when referencing this establishment in official correspondence.
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