Data / Medical devices / United States / BD Puerto Rico LLC
BD Puerto Rico LLC: FDA-registered device maker in Juncos, PR, United States, 20 510(k) clearances
BD Puerto Rico LLC is registered with the FDA (registration 2618282) in Juncos, PR, United States. It lists 14 device types. The FDA files 20 510(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
- 2618282
- FEI number
- 2649711
- Address
- RD 31, KM 24.3, Juncos, PR, United States, 00777
- Owner or operator
- Becton Dickinson and Company (9922032)
- Roles
- Manufacturer
- First device listed
- August 3, 2001
- Registered through
- 2026
- Brand names listed
- BD Arthrogram Tray, BD CytoRich Clear Collection Vial, BD Durasafe, BD Durasafe Combined Anesthesia Kit, BD Durasafe Plus, BD Epilor Syringe, BD INTERLINK CANNULA SYSTEMS, BD LUER TIP CAPS 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.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| April 10, 2026 | K252378 | BD® MiniDraw Capillary Blood Collection System with BD® MiniDraw SST Capillary Blood Collection Tube | JKA | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| December 1, 2023 | K230391 | BD MiniDraw Capillary Blood Collection System with BD MiniDraw SST Capillary Blood Collection Tube | JKA | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| November 27, 2023 | K230493 | BD MiniDraw Capillary Blood Collection System with BD MiniDraw H&H Capillary Blood Collection Tube | GIM | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| March 10, 2023 | K222478 | BD Vacutainer® Luer-Lok Access Device, BD Vacutainer® Blood Transfer Device | JKA | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| December 16, 2022 | K223243 | BD Microtainer® Contact-Activated Lancets; BD Microtainer® Quikheel Lancets | FMK | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| July 1, 2022 | K211085 | BD Perisafe Tuohy Epidural Needle, BD Perisafe Weiss Epidural Needle | BSP | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| May 19, 2022 | K210983 | BD Epilor Syringe | CAZ | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| December 22, 2021 | K210978 | BD Quincke Spinal Needle, BD Whitacre Spinal Needle, BD Spinal Introducer Needle | BSP | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| September 29, 2020 | K193131 | BD Quincke Spinal NRFit Needle, BD Whitacre Spinal NRFit Needle, BD Spinal Introducer NRFit Needle | BSP | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| October 9, 2009 | K091758 | BD SPINAL NEEDLE 27G | BSP | Substantially Equivalent | Becton Dickson & Co. | accessdata.fda.gov |
| November 2, 2000 | K002456 | MICROTAINER BRAND SODIUM FLUORIDE/EDTA TUBE WITH MICROGARD CLOSURE, MODEL 365992 | JKA | Substantially Equivalent | Becton Dickinson Vacutainer Systems | accessdata.fda.gov |
| July 28, 1999 | K991702 | MICROTAINER BRAND CHEMISTRY TUBES WITH MICROGARD CLOSURE, MODEL 365965, 365985, 365963, 365967, 36578 | JKA | Substantially Equivalent | Becton Dickinson Vacutainer Systems | accessdata.fda.gov |
| November 30, 1995 | K953790 | BD PERISAFE EPIDURAL ANESTHESIA TRAY | CAZ | Substantially Equivalent | Bd Becton Dickinson Vacutainer Systems Preanalytic | accessdata.fda.gov |
| August 2, 1994 | K940905 | MICROTAINER BRAND TUBE WITH EDTA(K2) | JKA | Substantially Equivalent | Bd Becton Dickinson Vacutainer Systems Preanalytic | accessdata.fda.gov |
| September 28, 1993 | K931368 | MICROTAINER BRAND TUBE WITH EDTA | JKA | Substantially Equivalent | Bd Becton Dickinson Vacutainer Systems Preanalytic | accessdata.fda.gov |
| August 27, 1993 | K932249 | DURASAFE B-D COMBINED SPINAL EPIDURAL ANESTHESIA | CAZ | Unknown | Bd Becton Dickinson Vacutainer Systems Preanalytic | accessdata.fda.gov |
| January 14, 1993 | K925902 | B-D LOSS OF RESISTANCE SYRINGE | CAZ | Substantially Equivalent | Bd Becton Dickinson Vacutainer Systems Preanalytic | accessdata.fda.gov |
| September 14, 1988 | K881697 | BREAST LESION LOCALIZATION NEEDLE | IZH | Substantially Equivalent | Bd Becton Dickinson Vacutainer Systems Preanalytic | accessdata.fda.gov |
| June 1, 1988 | K880988 | PUDENDAL/LOCAL ANESTESIA BLOCK TRAY | KNE | Substantially Equivalent | Bd Becton Dickinson Vacutainer Systems Preanalytic | accessdata.fda.gov |
| March 11, 1985 | K850505 | DESERET EPIDURAL CATHETER W/TOUGHY-BORST ADAPTER | BSO | Substantially Equivalent | Parke-Davis Co. | accessdata.fda.gov |
Compare with other makers
- All makers of Tubes, Vials, Systems, Serum Separators, Blood Collection
- All makers of Anesthesia Conduction Kit
- All makers of Needle, Conduction, Anesthetic (W/Wo Introducer)
- All makers of Dispenser, Liquid Medication
- All makers of Container, Specimen, Non-Sterile
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.