Data / Medical devices / Japan / JPS Corporation
JPS Corporation: FDA-registered device maker in Bunkyo City Tokyo, Japan, 1 510(k) clearance
JPS Corporation is registered with the FDA (registration 3027728077) in Bunkyo City Tokyo, Japan. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated January 22, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3027728077
- Address
- Toho Edogawabashi Bldg. 3F 1-24-8 Sekiguchi, Bunkyo City Tokyo, Japan, 112-0014
- Owner or operator
- JPS Corporation (10088545)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- January 30, 2024
- Registered through
- 2026
- Brand names listed
- NailLift
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Prosthesis, Nail | MQZ | U | Exporter to the US, 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 |
|---|---|---|---|---|---|---|
| January 22, 2024 | K230841 | NailLift | MQZ | Substantially Equivalent | Jps Corporation | accessdata.fda.gov |
Updated January 22, 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.