Benlan, Inc. is one of 461 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Benlan, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MED-RX ORAL/ENTERAL SYRINGE, MED-RX PATIENT DELIVERY SET, MED-RX EXTENSION SET WITH T-CONNECTOR
7
Total
7
Cleared
0
Denied
Benlan, Inc. has 7 FDA 510(k) cleared medical devices. Based in Oakville, CA.
Historical record: 7 cleared submissions from 1999 to 2014. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Benlan, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Benlan, Inc.
7 devices
Cleared
Jun 03, 2014
MED-RX ORAL/ENTERAL SYRINGE
Gastroenterology & Urology
403d
Cleared
Jun 28, 2012
MED-RX PATIENT DELIVERY SET
General Hospital
143d
Cleared
Dec 23, 2011
MED-RX EXTENSION SET WITH T-CONNECTOR
General Hospital
87d
Cleared
Dec 13, 2010
MED-RX PEDIATRIC FEEDING TUBES AND ACCESSORIES
Gastroenterology & Urology
276d
Cleared
Nov 08, 2010
MED-RX TRANSFER SET, MODELS 10-1227TS, 10-1300TS, 10-1305TS AND 10-1306TS
General Hospital
108d
Cleared
Nov 28, 2001
MED-RX IRRIGATION SET, MODEL 10-3001, 10-3002, 10-4000, 10-4001
Gastroenterology & Urology
272d
Cleared
Aug 25, 1999
MED-RX EXTENSION SETS
General Hospital
169d