Data / Medical devices / Japan / JMS Co., Ltd.
JMS Co., Ltd.: FDA-registered device maker in Hiroshima, Japan, 1 510(k) clearance
JMS Co., Ltd. is registered with the FDA (registration 8031563) in Hiroshima, Japan. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated February 20, 2014. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 8031563
- FEI number
- 1000162947
- Address
- 12-17, Kako-Machi, Naka-Ku, Hiroshima, Japan, 730-8652
- Owner or operator
- JMS CO., LTD. (8031563)
- Roles
- Exporter to the US
- First device listed
- August 20, 2015
- Registered through
- 2026
- Brand names listed
- DISPOSABLE SYRINGE, JMS Syringe
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Syringe, Piston | FMF | 2 | Exporter to the US | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| February 20, 2014 | K132321 | JMS SYRINGE | FMF | Substantially Equivalent | JMS North America Corporation | accessdata.fda.gov |
Compare with other makers
Updated February 20, 2014. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.