BECTON, DICKINSON & CO.

FDA Device Registration & Listing · San Diego, CA, US · Registration 3007886372

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
3007886372
FEI Number
3007886372
Entity Name
BECTON, DICKINSON & CO.
City/State/Country
San Diego, CA, US
Establishment Address
3750 Torrey View Ct, San Diego, CA 92130, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Becton Dickinson and Company (Owner Number: 9922032)
Owner / Operator Contact Address
One Becton Drive, Franklin Lakes, NJ 07417, 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 For Rapid Detection of Flu A+B Laboratory kit BD Veritor™ System For Rapid Detection of Flu A+B CLIA-waived kit BD Veritor™ System For Rapid Detection of RSV - Laboratory kit BD Veritor™ System For Rapid Detection of Flu A+B Laboratory kit BD Veritor™ System For Rapid Detection of Flu A+B Laboratory kit BD Veritor™ System for Rapid Detection of SARS-CoV-2 BD Veritor™ System For Rapid Detection of Flu A+B Laboratory kit BD Veritor™ System Group A Strep Control Swab set BD Veritor™ System RSV Control Swab Set BD Veritor™ System Flu A+B Control Swab Set BD Veritor™ SARS-CoV-2 Control Swab Set BD Veritor™ System For Rapid Detection of Flu A+B CLIA-waived kit BD Veritor™ System For Rapid Detection of Flu A+B Laboratory kit BD Veritor™ System For Rapid Detection of Flu A+B Laboratory kit BD Veritor™ System for Rapid Detection of Flu A+B CLIA-waived kit BD Veritor™ System For Rapid Detection of Flu A+B CLIA-waived kit BD Veritor™ System for Rapid Detection of Group A Strep CLIA-Waived Kit BD Veritor™ System For Rapid Detection of Flu A+B CLIA-waived kit BD Veritor™ System For Rapid Detection of Flu A+B CLIA-waived kit BD Veritor™ System For Rapid Detection of RSV - Laboratory kit BD Veritor™ System For Rapid Detection of Flu A+B CLIA-waived kit BD Veritor™ System for Rapid Detection of Flu A+B CLIA-waived kit BD Veritor™ System for Rapid Detection of SARS-CoV-2 & Flu A+B BD Veritor™ SARS-CoV-2 & Flu A+B Control Swab Set

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PSZ Devices Detecting Influenza A, B, And C Virus Antigens Microbiology Class 2 866.3328 2016-11-01
PSZ Devices Detecting Influenza A, B, And C Virus Antigens Microbiology Class 2 866.3328 2013-11-25
GQG Antigen, Cf (Including Cf Controls), Respiratory Syncytial Virus Microbiology Class 1 866.3480 2013-11-25
PSZ Devices Detecting Influenza A, B, And C Virus Antigens Microbiology Class 2 866.3328 2016-11-01
PSZ Devices Detecting Influenza A, B, And C Virus Antigens Microbiology Class 2 866.3328 2012-09-20
QVF Simple Point-Of-Care Device To Directly Detect Sars-Cov-2 Viral Targets From Clinical Specimens In Near-Patient Settings Microbiology Class 2 866.3982 2025-07-01
PSZ Devices Detecting Influenza A, B, And C Virus Antigens Microbiology Class 2 866.3328 2013-11-25
JJX Single (Specified) Analyte Controls (Assayed And Unassayed) Clinical Chemistry Class 1 862.1660 2017-12-12
PSZ Devices Detecting Influenza A, B, And C Virus Antigens Microbiology Class 2 866.3328 2013-11-25
PSZ Devices Detecting Influenza A, B, And C Virus Antigens Microbiology Class 2 866.3328 2013-11-25
PSZ Devices Detecting Influenza A, B, And C Virus Antigens Microbiology Class 2 866.3328 2013-11-25
PSZ Devices Detecting Influenza A, B, And C Virus Antigens Microbiology Class 2 866.3328 2025-12-11
PSZ Devices Detecting Influenza A, B, And C Virus Antigens Microbiology Class 2 866.3328 2018-06-04
GTY Antigens, All Groups, Streptococcus Spp. Microbiology Class 1 866.3740 2013-02-26
PSZ Devices Detecting Influenza A, B, And C Virus Antigens Microbiology Class 2 866.3328 2016-11-01
PSZ Devices Detecting Influenza A, B, And C Virus Antigens Microbiology Class 2 866.3328 2016-11-01
GQG Antigen, Cf (Including Cf Controls), Respiratory Syncytial Virus Microbiology Class 1 866.3480 2012-09-20
PSZ Devices Detecting Influenza A, B, And C Virus Antigens Microbiology Class 2 866.3328 2011-11-18
PSZ Devices Detecting Influenza A, B, And C Virus Antigens Microbiology Class 2 866.3328 2025-12-11
QMN Covid-19 Multi-Analyte Antigen Device Unknown Class N N/A 2021-03-30

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Becton Dickinson and Company
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
9680577 BECTON DICKINSON GMBH HEIDELBERG Baden-Wurttemberg, DE
3003916417 BECTON DICKINSON IND. CIRURGICAS LTDA. CURITIBA Parana, BR
3036495171 BD Biosciences San Diego San Diego, CA, US
3015292643 BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES San Diego, CA, US
3010141591 BD Kiestra B.V. Drachten Fryslan, NL

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K251289 Guangzhou Wondfo Biotech Co., Ltd. WELLlife COVID-19 Antigen Test Rx 2025-10-22
K103744 Quantimetrix Corp. DROPPER A1C DIABETES CONTROL 2011-05-12
K981281 Roche Diagnostics GmbH ELECSYS CALCHECK FERRITIN 1998-04-24
K981278 Roche Diagnostics GmbH ELECSYS CALCHECK CA 125II 1998-04-23
K143687 Siemens Healthcare Diagnostics, Inc. ADVIA Centaur Follicle Stimulating Hormone (FSH) Master Curve Material, ADVIA Centaur FT4 Master Curve Material, ADVIA Centaur T4 Master Curve Material, ADVIA Centaur T3 Master Curve Material 2015-07-17

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0022-2009 Becton Dickinson and Company 1
BD Visitec High Viscosity Injector, 4mm Ref: 585173. The product is intended for Vitroretinal Surgery.
Z-0007-2008 Tosoh Bioscience Inc 1
4 glass vials per box. 2/4ml vials of Sample Diluting Solution & 2/2ml vials of Calibration Verification Material. BetaHCG Calibration Verification Test Set, in vitro diagnostic.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007886372. Last updated year: 2026. Please use registration number 3007886372 when referencing this establishment in official correspondence.
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