Becton, Dickinson and Company (BD) is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Becton, Dickinson and Company (BD) - FDA 510(k) Cleared Devices
Recent clearances: BD Surgiphor™ Antimicrobial Irrigation System (910110)
5
Total
5
Cleared
0
Denied
Becton, Dickinson and Company (BD) has 5 FDA 510(k) cleared medical devices. Based in Vernon Hills, US.
Latest FDA clearance: Feb 2026. Active since 2009. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Becton, Dickinson and Company (BD) Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Becton, Dickinson and Company (BD)
5 devices
Cleared
Feb 25, 2026
BD Surgiphor™ Antimicrobial Irrigation System (910110)
General & Plastic Surgery
75d
Cleared
Oct 18, 2011
CEFTAROLINE 30 MICROGRAMS, BBL(TM) SENSI-DISC(TM)
Microbiology
42d
Cleared
Sep 30, 2011
BD NEXIVA DIFFUSICS CLOSED IV CATHETER SYSTEM
General Hospital
137d
Cleared
Apr 28, 2011
BD PEN NEEDLE
General Hospital
105d
Cleared
Aug 25, 2009
BD VACUTAINER RAPID SERUM TUBE PLUS BLOOD COLLECTION TUBE, MODEL 368771
Chemistry
113d