Data / Medical devices / System, X-Ray, Extraoral Source, Digital / Japan
FDA-registered makers of System, X-Ray, Extraoral Source, Digital in Japan: 6 establishments
6 establishments in Japan are registered with the FDA to make System, X-Ray, Extraoral Source, Digital (product code MUH). 2 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- System, X-Ray, Extraoral Source, Digital
- Product code
- MUH
- Country
- Japan
Makers of System, X-Ray, Extraoral Source, Digital in Japan
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| The Yoshida Dental MFG. Co., Ltd. | Tokyo, Japan | Manufacturer | 3 | January 31, 2019 | 0 | 0 | 0 | api.fda.gov |
| J. Morita MFG. Corp. | FUSHIMI-KU Kyoto, Japan | Manufacturer | 2 | April 8, 2008 | 0 | 0 | 0 | api.fda.gov |
| J. Morita MFG. Corp., Tottori Factory | Kurayoshi Tottori, Japan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MD Instruments MFG. Co.,ltd. | Inashiki-Gun Ibaraki, Japan | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Takara Belmont Corporation | Osaka, Japan | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Takara Medical Co., Ltd. | Amagasaki Hyogo, Japan | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 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.