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Data / Medical devices / United States / Becton, Dickinson & Co., (BD)

Becton, Dickinson & Co., (BD): FDA-registered device maker in Sumter, SC, United States, 7 510(k) clearances

Becton, Dickinson & Co., (BD) is registered with the FDA (registration 1024879) in Sumter, SC, United States. It lists 6 device types. The FDA files 7 510(k) clearances under its listings, the newest dated April 10, 2026. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
1024879
Address
1575 Airport Rd, Sumter, SC, United States, 29153
Owner or operator
Becton Dickinson and Company (9922032)
Roles
Contract sterilizer, Manufacturer, Repackager or relabeler
First device listed
August 3, 2001
Registered through
2026
Brand names listed
BD BACTEC™ Subculturing/Aerobic Venting Unit, BD BBL™ Venting Unit, BD Blunt Fill NRFit Needle, BD Blunt Fill Needle, BD Blunt Filter NRFit Needle, BD Blunt Filter Needle, BD Nokor Needle, BD Serum Separation Tubes and more

Devices it lists

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
April 10, 2026K252506BD Vacutainer® Safety-Lok™ Blood Collection Set; BD Vacutainer® Safety-Lok™ Blood Collection Set with Pre-Attached HolderJKASubstantially EquivalentBecton, Dickinson and Companyaccessdata.fda.gov
July 3, 2025K243207BD Vacutainer® Eclipse™ Blood Collection NeedleJKASubstantially EquivalentBecton, Dickinson and Companyaccessdata.fda.gov
March 21, 2025K243649BD Vacutainer® Multiple Sample Luer AdapterJKASubstantially EquivalentBecton, Dickinson and Companyaccessdata.fda.gov
December 20, 2023K230855BD Vacutainer® Serum Separator (SST™) Blood Collection TubesJKASubstantially EquivalentBecton, Dickinson and Companyaccessdata.fda.gov
March 24, 2023K220212BD Vacutainer® Push Button Blood Collection Set, BD Vacutainer® Push Button Blood Collection Set with Pre-Attached HolderJKASubstantially EquivalentBecton, Dickinson and Companyaccessdata.fda.gov
February 4, 2022K212724BD Vacutainer UltraTouch Push Button Blood Collection SetJKASubstantially EquivalentBecton, Dickinson and Companyaccessdata.fda.gov
March 29, 1996K960250VACUTAINER BRAND PLUS SERUM & SST TUBESJKASubstantially EquivalentBecton Dickinson Vacutainer Systemsaccessdata.fda.gov

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Updated April 10, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.