Medical Device Manufacturer · US , Crofton , MD

JMS North America Corporation

9 submissions · 9 cleared · Since 2011

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.

9 devices

1–9 of 9

JMS CAVEO A.V. Fistula Needle Set

K251877 · FIE Needle, Fistula · Gastroenterology & Urology

K172499 · ONB Closed Antineoplastic And Hazardous Drug Reconstitution And Transfer System · General Hospital

JMS Harmony A.V. Fistula Needle Set

K151017 · FIE Needle, Fistula · Gastroenterology & Urology

JMS SysLoc MINI A.V. Fistula Needle Set (V4), JMS SysLoc MINI Apheresis Needle Set (V4)

K142564 · FIE Needle, Fistula · Gastroenterology & Urology

K132321 · FMF Syringe, Piston · General Hospital

JMS SAFE WING CATH (SWC)

K121488 · FOZ Catheter, Intravascular, Therapeutic, Short-term Less Than 30 Days · General Hospital

JMS APHERESIS NEEDLE SET WINGEATER(R) V2

K112178 · FIE Needle, Fistula · Gastroenterology & Urology

K111948 · FIE Needle, Fistula · Gastroenterology & Urology

K110157 · FIE Needle, Fistula · Gastroenterology & Urology