Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1911916

FEI Number

1911916

Entity Name

BECTON DICKINSON AND COMPANY

City/State/Country

COLUMBUS, NE, US

Establishment Address

2153 12th Ave, COLUMBUS, NE 68601, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Becton Dickinson and Company (Owner Number: 9922032)

Owner / Operator Contact Address

One Becton Drive, Franklin Lakes, NJ 07417, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Heparin Lock Flush Solution, USP- BD PosiFlush Heparin Lock Flush Syringe BD PosiFlush PureHub Disinfecting Cap Interlink Vial Access Cannula BD PosiFlush Heparin BD Intramedic Luer-Stub Adapter BD LUER TIP CAPS BD ORAL TIP CAPS BD ORAL SYRINGES Twinpak BD Integra BD PosiFlush Secondary Sets BD Hypodermic Needles BD PrecisionGlide Needle BD Nokor Needle BD Blunt Filter NRFit Needle BD Blunt Fill NRFit Needle BD Blunt Filter Needle BD Blunt Fill Needle BD SafetyGlide Needle BD Syringe BD Oral/Enteral Syringe BD PosiFlush SafeScrub Alcohol Swab BD Catheter Tip Syringe BD INTERLINK CANNULA SYSTEMS BECTON DICKINSON INTE

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NZW	Heparin, Vascular Access Flush	General Hospital	Class 2	880.5200	2020-12-09
NGT	Saline, Vascular Access Flush	General Hospital	Class 2	880.5200	2014-09-19
QBP	Cap, Device Disinfectant	General Hospital	Class 2	880.5440	2020-11-09
FMI	Needle, Hypodermic, Single Lumen	General Hospital	Class 2	880.5570	2008-03-05
NZW	Heparin, Vascular Access Flush	General Hospital	Class 2	880.5200	2009-06-23
KGZ	Accessories, Catheter	General, Plastic Surgery	Class 1	878.4200	2004-12-28
KYW	Container, Liquid Medication, Graduated	General Hospital	Class 1	880.6430	2001-08-03
FMI	Needle, Hypodermic, Single Lumen	General Hospital	Class 2	880.5570	2008-03-05
FMF	Syringe, Piston	General Hospital	Class 2	880.5860	2008-02-19
MEG	Syringe, Antistick	General Hospital	Class 2	880.5860	2008-02-19
NGT	Saline, Vascular Access Flush	General Hospital	Class 2	880.5200	2019-04-01
FPA	Set, Administration, Intravascular	General Hospital	Class 2	880.5440	2015-10-05
JKA	Tubes, Vials, Systems, Serum Separators, Blood Collection	Clinical Chemistry	Class 2	862.1675	2008-02-19
FMI	Needle, Hypodermic, Single Lumen	General Hospital	Class 2	880.5570	2008-02-19
FMF	Syringe, Piston	General Hospital	Class 2	880.5860	2008-02-19
GAA	Needle, Aspiration And Injection, Disposable	General, Plastic Surgery	Class 1	878.4800	2001-08-03
FMI	Needle, Hypodermic, Single Lumen	General Hospital	Class 2	880.5570	2007-12-10
FMF	Syringe, Piston	General Hospital	Class 2	880.5860	2013-06-03
KNT	Tubes, Gastrointestinal (And Accessories)	Gastroenterology, Urology	Class 2	876.5980	2011-12-12
QTI	Saline Vascular Access Flush With Integrated Alcohol Disinfectant Device	General Hospital	Class 2	880.5200	2022-08-09
LKB	Pad, Alcohol, Device Disinfectant	Unknown	Class U	N/A	2013-04-25
KYZ	Syringe, Irrigating (Non Dental)	General Hospital	Class 1	880.6960	2001-08-03
FGY	Cannula, Injection	General, Plastic Surgery	Class 1	878.4200	2001-08-29

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
K812404	Nu Tech Medical Systems	BUTTERFLY NEEDLE ASSEMBLY	1981-09-09
K880350	Honway International Co.	YUE/FA DISPOSABLE SYRINGE	1988-02-16
K003571	Terumo Medical Corp.	SERONO FOR USE WITH GONAL-F 1200IU MULTI-DOSE ONLY AT 600IU/ML SYRINGE	2001-02-12
K092413	Inviro Medical Devices, Inc.	INVIROSNAP 50 AND 100 UNIT INSULIN SAFETY SYRINGES	2009-09-04
K163162	Jiangxi Hongda Medical Equipment Group , Ltd.	Sterile Hypodermic Safety Syringes for Single Use	2017-03-20

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-0035-2011	Excelsior Medical Corp	2	Excelsior Disposable Syringe W/Normal Saline (0.9% sodium Chloride) General hospital use
Z-0044-2007	Excelsior Medical Corp	2	0.9% Sodium Chloride Flush Syringe, 2.5 mL. Product Code: E0100-30. Manufactured by Excelsior Medical and distributed by Hospira, Lake Forest, IL under Hospira''s label, Syrex.
Z-0002-2022	Bard Peripheral Vascular Inc	2	REF TIN3015, 15G x 79 mm Bone Marrow Aspiration/Intraosseous Infusion Needle, For Single Use Only, Sterile EO, UDI: 10885403043796
Z-0003-04	Liberty Medical Supplies	2	Liberty brand Insulin Syringes for use with U-100 insulin, 1/2 cc X 30G X 5/16'' syringes

Similar Registrations

Registration Number	Establishment Name	Location
2243072	BECTON DICKINSON	FRANKLIN LAKES, NJ, US
1423982	MEDEFIL, INC.	GLENDALE HEIGHTS, IL, US
3012421607	MAINLINE MEDICAL DENTAL SUPPLY	North York Ontario, CA
3008518459	EXCELSIOR MEDICAL LLC	Freehold, NJ, US
2027791	EXCELSIOR MEDICAL LLC	NEPTUNE, NJ, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1911916. Last updated year: 2026. Please use registration number 1911916 when referencing this establishment in official correspondence.