Data / Medical devices / Vietnam / B And B Investment Company Limited
B And B Investment Company Limited: FDA-registered device maker in Ha Dong Ward Ha Noi, Vietnam, 10 510(k) clearances
B And B Investment Company Limited is registered with the FDA (registration 3042871620) in Ha Dong Ward Ha Noi, Vietnam. It lists 6 device types. The FDA files 10 510(k) clearances under its listings, the newest dated April 10, 2026. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3042871620
- Address
- B-TT9-2 Him Lam Van Phuc Residential Area, Ha Dong Ward Ha Noi, Vietnam, 10000
- Owner or operator
- B And B Investment Company Limited (10094922)
- Roles
- Exporter to the US
- First device listed
- January 6, 2026
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Post, Root Canal | ELR | 1 | Exporter to the US | accessdata.fda.gov |
| Set, Administration, Intravascular | FPA | 2 | Exporter to the US | accessdata.fda.gov |
| Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature | FMK | 2 | Exporter to the US | accessdata.fda.gov |
| Tape And Bandage, Adhesive | KGX | 1 | Exporter to the US | accessdata.fda.gov |
| Tubes, Vacuum Sample, With Anticoagulant | GIM | 2 | Exporter to the US | accessdata.fda.gov |
| Tubes, Vials, Systems, Serum Separators, Blood Collection | JKA | 2 | Exporter to the US | 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 10, 2026 | K252506 | BD Vacutainer® Safety-Lok Blood Collection Set; BD Vacutainer® Safety-Lok Blood Collection Set with Pre-Attached Holder | JKA | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| March 13, 2026 | K252040 | BD Vacutainer® Plasma Separator Tubes (PST), BD Vacutainer® Sodium Heparin Blood Collection Tubes | JKA | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| March 21, 2025 | K243649 | BD Vacutainer® Multiple Sample Luer Adapter | JKA | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| January 19, 2024 | K231237 | BD Vacutainer® Fluoride Blood Collection Tubes | JKA | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| July 17, 2023 | K213953 | BD Vacutainer® Trace Element K2EDTA Tubes, BD Vacutainer® Trace Element Serum Tubes | 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 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 |
| 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 |
| December 27, 1993 | K932422 | 3M TEGADERM HP TRANSPARENT DRESSING | KGX | Substantially Equivalent | 3M Health Care, Ltd. | accessdata.fda.gov |
| July 23, 1990 | K901845 | TEGADERM BRAND TRANSPARENT DRESSING SERIES 16XX | KGX | Substantially Equivalent for Some Indications | 3M Company | accessdata.fda.gov |
Compare with other makers
- All makers of Tubes, Vials, Systems, Serum Separators, Blood Collection
- All makers of Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature
- All makers of Set, Administration, Intravascular
- All makers of Post, Root Canal
- All makers of Tape And Bandage, Adhesive
- All makers of Tubes, Vacuum Sample, With Anticoagulant
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.