JMS North America Corporation - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
JMS North America Corporation has 9 FDA 510(k) cleared medical devices. Based in Crofton, US.
Latest FDA clearance: Aug 2025. Active since 2011. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by JMS North America Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by JMS North America Corporation
9 devices
Cleared
Aug 15, 2025
JMS CAVEO A.V. Fistula Needle Set
Gastroenterology & Urology
58d
Cleared
Jun 01, 2018
NEOSHIELD
General Hospital
287d
Cleared
May 13, 2015
JMS Harmony A.V. Fistula Needle Set
Gastroenterology & Urology
27d
Cleared
Dec 23, 2014
JMS SysLoc MINI A.V. Fistula Needle Set (V4), JMS SysLoc MINI Apheresis...
Gastroenterology & Urology
103d
Cleared
Feb 20, 2014
JMS SYRINGE
General Hospital
210d
Cleared
Mar 05, 2013
JMS SAFE WING CATH (SWC)
General Hospital
291d
Cleared
Oct 27, 2011
JMS APHERESIS NEEDLE SET WINGEATER(R) V2
Gastroenterology & Urology
91d
Cleared
Oct 24, 2011
WINGEATER V2
Gastroenterology & Urology
108d
Cleared
Feb 11, 2011
SYSLOC MINI V3
Gastroenterology & Urology
23d