Jabil Circuit Sdn. Bhd.

FDA Device Registration & Listing · Bayan Lepas Pulau Pinang, MY · Registration 3011246727

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
3011246727
FEI Number
3011246727
Entity Name
Jabil Circuit Sdn. Bhd.
City/State/Country
Bayan Lepas Pulau Pinang, MY
Establishment Address
56, Hilir Sungai Keluang 1, Bayan Lepas Industrial Park, Phase 4, Bayan Lepas Pulau Pinang 11900, MY
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Jabil Inc. (Owner Number: 9074019)
Owner / Operator Contact Address
10800 Roosevelt Blvd., Saint Petersburg, FL 33716, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

BD Veritor System Reader BD Veritor Plus System Analyzer

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JJQ Colorimeter, Photometer, Spectrophotometer For Clinical Use Clinical Chemistry Class 1 862.2300 2017-11-10

Official Correspondent

No official correspondent registered.

US Agent Details

Lex Pearce Business: JABIL - NYPRO HEALTHCARE DIVISION Email: lex_pearce@jabil.com Phone: (505) 2030277

Related Public Records

Same Entity

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

Other Registrations for Same Entity

Registration Number Establishment Name Location
3015410662 Jabil Inc. (Wilson Drive) W Chester, PA, US
3003512059 NYPRO DR, LLC (Bldg 11) Haina San Cristobal, DO
3004730544 NYPRO DR, LLC (Building 52) Haina San Cristobal, DO
1424235 Nypro Inc. (Chicago) GURNEE, IL, US
3010972758 Jabil Circuit (Shanghai) Ltd. Shanghai, CN

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K760232 Instrumentation Laboratory CO PRINTER, IL 460 1976-08-26

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011246727. Last updated year: 2026. Please use registration number 3011246727 when referencing this establishment in official correspondence.
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