Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008336863

FEI Number

3008336863

Entity Name

AB SCIEX LP

City/State/Country

Concord Ontario, CA

Establishment Address

71 Four Valley Drive, Concord Ontario L4K 4V8, CA

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198

Owner / Operator

AB SCIEX (Owner Number: 10041672)

Owner / Operator Contact Address

71 Four Valley Drive, Concord, CA-ON L4K4V8, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

3200MD QTRAP® LC/MS/MS System AB SCIEX QTRAP® 4500MD Citrine QTRAP MS/MS Citrine Triple Quad MS/MS AB SCIEX Triple Quad 4500MD API 3200MD LC/MS/MS System

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DOP	Mass Spectrometer, Clinical Use	Clinical Chemistry	Class 1	862.2860	2012-08-20

Official Correspondent

Christine Huynh

US Agent Details

Brenda Newton Business: AB SCIEX Email: brenda.newton@sciex.com Phone: (508) 3837700

Related Public Records

Same Entity

AB SCIEX

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3009715051	AB SCIEX Pte. Ltd.	Woodlands Central Industrial Estate Central Singapore, SG

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0037-2024	AB Sciex, LLC	1	API3200MD Mass Spectrometer, Part Number 4466230
Z-0038-2024	AB Sciex, LLC	1	4500MD Triple Quad Mass Spectrometer, Part Number 5032522
Z-0039-2024	AB Sciex, LLC	1	Citrine QTRAP Mass Spectrometer, Part Number 5063685
Z-0040-2024	AB Sciex, LLC	1	Citrine Triple Quad Mass Spectrometer, Part Number 5063684

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008336863. Last updated year: 2026. Please use registration number 3008336863 when referencing this establishment in official correspondence.