Data / Medical devices / Japan / JMS Co.,Ltd. Miyoshi Plant
JMS Co.,Ltd. Miyoshi Plant: FDA-registered device maker in Miyoshi Hiroshima, Japan, 1 510(k) clearance
JMS Co.,Ltd. Miyoshi Plant is registered with the FDA (registration 3009249481) in Miyoshi 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
- 3009249481
- Address
- 350 Yamaga, Shijikkan-machi, Miyoshi Hiroshima, Japan, 728-0016
- Owner or operator
- JMS CO., LTD. (8031563)
- Roles
- Manufacturer
- 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 | Manufacturer | 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.