JMS North America Corporation
JMS North America Corporation appears in FDA public data with 0 recalls, 9 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 15, 2025.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K251877 | JMS CAVEO A.V. Fistula Needle Set | August 15, 2025 |
| K172499 | NEOSHIELD | June 1, 2018 |
| K151017 | JMS Harmony A.V. Fistula Needle Set | May 13, 2015 |
| K142564 | JMS SysLoc MINI A.V. Fistula Needle Set (V4), JMS SysLoc MINI Apheresis Needle Set (V4) | December 23, 2014 |
| K132321 | JMS SYRINGE | February 20, 2014 |
| K121488 | JMS SAFE WING CATH (SWC) | March 5, 2013 |
| K112178 | JMS APHERESIS NEEDLE SET WINGEATER(R) V2 | October 27, 2011 |
| K111948 | WINGEATER V2 | October 24, 2011 |
| K110157 | SYSLOC MINI V3 | February 11, 2011 |