Bd is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bd - FDA 510(k) Cleared Devices
Recent clearances: BD Surgiphor™ 1000 mL Antimicrobial Irrigation System (910120), Denali™ Vena Cava Filter System – Femoral and Jugular/Subclavian Delivery Kit, BD Veritor™ System for Rapid Detection of Flu A+B CLIA Waived Kit
15
Total
15
Cleared
0
Denied
Bd has 15 FDA 510(k) cleared medical devices. Based in Vernon Hills, US.
Latest FDA clearance: Feb 2026. Active since 2001. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Bd Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bd
15 devices
Cleared
Feb 20, 2026
BD Surgiphor™ 1000 mL Antimicrobial Irrigation System (910120)
General & Plastic Surgery
141d
Cleared
Feb 29, 2024
Denali™ Vena Cava Filter System – Femoral and Jugular/Subclavian Delivery Kit
Cardiovascular
29d
Cleared
Dec 05, 2023
BD Veritor™ System for Rapid Detection of Flu A+B CLIA Waived Kit
Microbiology
116d
Cleared
Jan 27, 2023
BD VeritorTM System for Rapid Detection of Flu A+B CLIA-Waived Kit
Microbiology
120d
Cleared
Oct 14, 2022
BD Surgiphor™ Antimicrobial Irrigation System
General & Plastic Surgery
144d
Cleared
Mar 20, 2018
BD Veritor System for Rapid Detection of Flu A + B CLIA waived kit
Microbiology
28d
Cleared
Mar 26, 2003
BD VACUTAINER PLUS PLASTIC URINE C&S PRESERVAYIVE TUBES AND KITS
Microbiology
93d
Cleared
Feb 07, 2003
BD INTEGRA SYRINGE
General Hospital
91d
Cleared
Jul 19, 2002
BD SINGLE LUMEN NEEDLE, SYRINGE AND BLOOD COLLECTION SET
General Hospital
72d
Cleared
Mar 20, 2002
BD BIFURCATED NEEDLE, MODELS 301754, 301755, 301756, 301757
General Hospital
29d
Cleared
Jan 23, 2002
BD PRE-FILLED HEPARIN LOCK FLUSH IN 0.9% SODIUM CHLORIDE INJECTION, USP SYRINGE
General Hospital
212d
Cleared
Sep 06, 2001
MODIFICATION TO: BD DURASAFE PLUS EPIDURAL LOCK CSE NEEDLE SET/KIT
Anesthesiology
27d