Data / Medical devices / Solid State X-Ray Imager (Flat Panel/Digital Imager) / Japan
FDA-registered makers of Solid State X-Ray Imager (Flat Panel/Digital Imager) in Japan: 12 establishments
12 establishments in Japan are registered with the FDA to make Solid State X-Ray Imager (Flat Panel/Digital Imager) (product code MQB). 12 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Solid State X-Ray Imager (Flat Panel/Digital Imager)
- Product code
- MQB
- Country
- Japan
Makers of Solid State X-Ray Imager (Flat Panel/Digital Imager) in Japan
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Canon Components, Inc. | KODAMA-GUN Saitama, Japan | Manufacturer | 19 | October 17, 2022 | 0 | 0 | 0 | api.fda.gov |
| Canon Inc. | Kawasaki Kanagawa, Japan | Specification developer | 19 | October 17, 2022 | 0 | 1 | 0 | api.fda.gov |
| Canon.Inc | OHTA-KU Tokyo, Japan | Specification developer | 19 | October 17, 2022 | 0 | 0 | 0 | api.fda.gov |
| Konica Minolta, Inc. | HINO-SHI Tokyo, Japan | Complaint file establishment, Specification developer | 19 | June 17, 2025 | 0 | 0 | 0 | api.fda.gov |
| Konica Minolta Technoproducts Co., Ltd. | SAYAMA-SHI Saitama, Japan | Manufacturer | 18 | June 17, 2025 | 0 | 0 | 0 | api.fda.gov |
| Konica Minolta, Inc. | HACHIOJI-SHI Tokyo, Japan | Specification developer | 18 | June 17, 2025 | 0 | 0 | 0 | api.fda.gov |
| Fujifilm Corporation | ASHIGARAKAMI-GUN Kanagawa, Japan | Complaint file establishment, Manufacturer | 9 | April 10, 2020 | 0 | 0 | 0 | api.fda.gov |
| FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office | HANAMAKI-SHI Iwate, Japan | Manufacturer | 7 | April 10, 2020 | 0 | 0 | 0 | api.fda.gov |
| Canon Inc. | OTAWARA-SHI Tochigi, Japan | Manufacturer | 3 | October 9, 2012 | 0 | 0 | 0 | api.fda.gov |
| Canon Inc. | OHTA-KU Tokyo, Japan | Specification developer | 3 | October 9, 2012 | 0 | 0 | 0 | api.fda.gov |
| FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Takematsu Office | MINAMIASHIGARA-SHI Kanagawa, Japan | Manufacturer | 1 | August 25, 2004 | 0 | 0 | 0 | api.fda.gov |
| Shimadzu Corporation Medical Systems Division | Kyoto, Japan | Complaint file establishment, Manufacturer | 1 | June 1, 2005 | 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.