ADVANCED ENGINEERING, INC.

FDA Device Registration & Listing · Huntington, IN, US · Registration 3010047203

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
3010047203
FEI Number
3010047203
Entity Name
ADVANCED ENGINEERING, INC.
City/State/Country
Huntington, IN, US
Establishment Address
5299 N Mishler Rd, Huntington, IN 46750, US
Establishment Type(s)
Manufacture Device in the United States for Export Only
Owner / Operator
Advanced Engineering, Inc. (Owner Number: 10042897)
Owner / Operator Contact Address
5299 N. Mishler Rd., Huntington, IN 46750, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Biocue Platelet Conc. System Biocue Platelet Conc. System CENTRIFUGE & ACCESSORY GPS II and Plasmax with 30ml ACD-A GPS III - std, mini, double, kits, Plasmax w/GPS III mini, Plasmax Plus w/GPS III GPS II Platelet Concentrate Separation Kit Marrowstim Concentration Kits nSTRIDE APS Kit (800-3000ST), APS Kit (800-3000JP)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JQC Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use Clinical Chemistry Class 1 862.2050 2013-01-09
JQC Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use Clinical Chemistry Class 1 862.2050 2013-01-09
JQC Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use Clinical Chemistry Class 1 862.2050 2021-12-13
KSS Supplies, Blood-Bank Hematology Class 1 864.9050 2013-01-09
KSS Supplies, Blood-Bank Hematology Class 1 864.9050 2013-01-09
KSS Supplies, Blood-Bank Hematology Class 1 864.9050 2013-01-09
JQC Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use Clinical Chemistry Class 1 862.2050 2013-01-09
PZT Peripheral Blood Processing Device For Osteoarthritis Unknown Class N N/A 2017-12-14

Official Correspondent

Frances Stouffer

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Advanced Engineering, 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 3010047203. Last updated year: 2026. Please use registration number 3010047203 when referencing this establishment in official correspondence.
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