Data / Medical devices / United Kingdom / Becton, Dickinson & Company (BD)
Becton, Dickinson & Company (BD): FDA-registered device maker in Plymouth Devon, United Kingdom, 12 510(k) clearances
Becton, Dickinson & Company (BD) is registered with the FDA (registration 9617032) in Plymouth Devon, United Kingdom. It lists 7 device types. The FDA files 12 510(k) clearances under its listings, the newest dated April 15, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9617032
- FEI number
- 3002806485
- Address
- BELLIVER INDUSTRIAL ESTATE Belliver Way, Plymouth Devon, United Kingdom, PL6 7BP
- Owner or operator
- Becton Dickinson and Company (9922032)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- September 13, 1994
- Registered through
- 2026
- Brand names listed
- BD A-Line, BD Preset Eclipse, BD Preset and BD A-Line Arterial Blood Collection Syringes, BD Seditainer Stand, BD VACUTAINER NO ADDIT, BD Vacutainer EDTA Tubes, BD Vacutainer Histology Specimen Container, BD Vacutainer Plastic Citrate Tube and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Blood/Plasma Collection Device For Dna Testing | PJE | 2 | Contract manufacturer | accessdata.fda.gov |
| Container, Specimen Mailer And Storage, Sterile | KDT | 1 | Manufacturer | accessdata.fda.gov |
| Container, Specimen, Sterile | FMH | 1 | Manufacturer | accessdata.fda.gov |
| Set, Administration, Intravascular | FPA | 2 | Manufacturer | accessdata.fda.gov |
| System, Blood Collection, Rna Stabilization, Rna Purification, Rt-Pcr Molecular Diagnostic Test | NTW | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Tubes, Vacuum Sample, With Anticoagulant | GIM | 2 | Manufacturer | accessdata.fda.gov |
| Tubes, Vials, Systems, Serum Separators, Blood Collection | JKA | 2 | Manufacturer | accessdata.fda.gov |
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.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| April 15, 2026 | K260128 | BD Preset and BD A-Line Arterial Blood Collection Syringes | JKA | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| February 2, 2024 | K231373 | BD Vacutainer® K2 EDTA Blood Collection Tubes | JKA | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| August 25, 2023 | K213670 | BD Vacutainer K2EDTA Blood Collection Tubes, BD Vacutainer K3EDTA Blood Collection Tubes | GIM | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| March 24, 2023 | K220212 | BD Vacutainer® Push Button Blood Collection Set, BD Vacutainer® Push Button Blood Collection Set with Pre-Attached Holder | JKA | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| February 4, 2022 | K212724 | BD Vacutainer UltraTouch Push Button Blood Collection Set | JKA | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| September 25, 2020 | K202446 | BD Preset Syringe & BD A-Line Syringe | JKA | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| September 23, 2016 | K160657 | BD Vacutainer Barricor Lithium Heparin Plasma Blood Collection Tube | JKA | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| February 4, 2009 | K082150 | MODIFICATION TO PAXGENE BLOOD RNA SYSTEM | NTW | Substantially Equivalent | Preanalytix GmbH | accessdata.fda.gov |
| February 1, 2002 | K013971 | BD VACUTAINER SAFETY COAGULATION TUBE | JKA | Substantially Equivalent | Becton, Dickinson & CO | accessdata.fda.gov |
| May 19, 1999 | K991120 | VACUTAINER BRAND CTAD TUBE (MULTIPLE) | JKA | Substantially Equivalent | Becton Dickinson Vacutainer Systems | accessdata.fda.gov |
| June 17, 1998 | K981013 | VACUTAINER PLUS TUBE WITH EDTA ANTICOAGULANT ANDD VACUTAINER PLUS SERUM TUBE | JKA | Substantially Equivalent for Some Indications | Becton Dickinson Vacutainer Systems | accessdata.fda.gov |
| September 26, 1995 | K953994 | SEDITAINER* ERYTHROCYTE SEDIMENTATION RATE (ESR) SYSTEM | JKA | Substantially Equivalent | Becton Dickinson Vacutainer Systems | accessdata.fda.gov |
Compare with other makers
- All makers of Tubes, Vials, Systems, Serum Separators, Blood Collection
- All makers of Set, Administration, Intravascular
- All makers of Blood/Plasma Collection Device For Dna Testing
- All makers of Tubes, Vacuum Sample, With Anticoagulant
- All makers of System, Blood Collection, Rna Stabilization, Rna Purification, Rt-Pcr Molecular Diagnostic Test
- All makers of Container, Specimen, Sterile
Updated April 15, 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.