Data / Medical devices / System, Nuclear Magnetic Resonance Imaging / Japan
FDA-registered makers of System, Nuclear Magnetic Resonance Imaging in Japan: 5 establishments
5 establishments in Japan are registered with the FDA to make System, Nuclear Magnetic Resonance Imaging (product code LNH). 4 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Device
- System, Nuclear Magnetic Resonance Imaging
- Product code
- LNH
- Country
- Japan
Makers of System, Nuclear Magnetic Resonance Imaging in Japan
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Canon Inc. | OTAWARA-SHI Tochigi, Japan | Manufacturer | 49 | March 27, 2026 | 0 | 0 | 0 | api.fda.gov |
| Canon Inc. | OHTA-KU Tokyo, Japan | Specification developer | 49 | March 27, 2026 | 0 | 0 | 0 | api.fda.gov |
| FUJIFILM Corporation Medical Systems Research & Development Center Kashiwa | KASHIWA-SHI Chiba, Japan | Manufacturer | 13 | September 16, 2026 | 0 | 0 | 0 | api.fda.gov |
| FUJIFILM Healthcare Manufacturing Corporation Kashiwa Office | Kashiwa-shi Chiba, Japan | Manufacturer | 13 | September 16, 2026 | 0 | 0 | 0 | api.fda.gov |
| Ziosoft, Inc. | Minato-ku Tokyo, Japan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 2026. 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.