Medionics International, Inc. is one of 201 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Medionics International, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Medionics International, Inc. has 4 FDA 510(k) cleared medical devices. Based in Markham, Ontario, CA.
Historical record: 4 cleared submissions from 1995 to 2013. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Medionics International, Inc. Filter by specialty or product code using the sidebar.
Medionics International, Inc. — FDA 510(k) Products and Clearance History
4 devices
Cleared
Apr 19, 2013
FALLER STYLET
Gastroenterology & Urology
57d
Cleared
Apr 28, 2000
PERITONEAL DIALYSIS CATHETERS AND ADAPTERS
Gastroenterology & Urology
220d
Cleared
Feb 10, 2000
EASY CARE AND TUBING SETS
Gastroenterology & Urology
57d
Cleared
Feb 07, 1995
QC CAP
Gastroenterology & Urology
133d