Data / Medical devices / Japan / Mochida Pharmaceutical Co., Ltd
Mochida Pharmaceutical Co., Ltd: FDA-registered device maker in Shinjuku-ku Tokyo, Japan, 1 510(k) clearance
Mochida Pharmaceutical Co., Ltd is registered with the FDA (registration 9612125) in Shinjuku-ku Tokyo, Japan. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 21, 2024. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 9612125
- FEI number
- 3002807644
- Address
- 1-7, Yotsuya, Shinjuku-ku Tokyo, Japan, 1608515
- Owner or operator
- Mochida Pharmaceutical Co., LTD (10091242)
- Roles
- Complaint file establishment
- First device listed
- August 28, 2024
- Registered through
- 2027
- Brand names listed
- ReFeel
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cuff, Nerve | JXI | 2 | Complaint file establishment | 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 |
|---|---|---|---|---|---|---|
| June 21, 2024 | K233322 | Mochida Nerve Cuff | JXI | Substantially Equivalent | Mochida Pharmaceutical Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated June 21, 2024. 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.