Data / Medical devices / Solid State X-Ray Imager (Flat Panel/Digital Imager) / China
FDA-registered makers of Solid State X-Ray Imager (Flat Panel/Digital Imager) in China: 14 establishments
14 establishments in China are registered with the FDA to make Solid State X-Ray Imager (Flat Panel/Digital Imager) (product code MQB). 7 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 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
- Solid State X-Ray Imager (Flat Panel/Digital Imager)
- Product code
- MQB
- Country
- China
Makers of Solid State X-Ray Imager (Flat Panel/Digital Imager) in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| iRay Group | Shanghai, China | Complaint file establishment, Manufacturer, Specification developer | 15 | February 3, 2023 | 0 | 0 | 0 | api.fda.gov |
| Careray Digital Medical Technology Co., Ltd. | SuZhou Jiangsu, China | Manufacturer | 13 | August 3, 2023 | 0 | 0 | 0 | api.fda.gov |
| GE Healthcare (China) Co., Ltd. | Beijing, China | Specification developer | 2 | November 18, 2010 | 0 | 0 | 0 | api.fda.gov |
| Pzmedical Technology Co., Ltd. | Putuo District Shanghai, China | Manufacturer | 2 | August 23, 2021 | 0 | 0 | 0 | api.fda.gov |
| Carestream Health, Inc., Global R&D Center | Shanghai, China | Specification developer | 1 | October 16, 2019 | 0 | 0 | 0 | api.fda.gov |
| FUJIFILM Imaging System (Suzhou) Co., Ltd. | Suzhou Jiangsu, China | Manufacturer | 1 | August 25, 2004 | 0 | 0 | 0 | api.fda.gov |
| Ge Hangwei Medical Systems Co., Ltd. | Beijing, China | Manufacturer | 1 | November 18, 2010 | 0 | 0 | 0 | api.fda.gov |
| Philips Healthcare (Suzhou) Co., Ltd. | Suzhou Jiangsu, China | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shanghai United Imaging Healthcare Co.,ltd. | Shanghai, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shantou Institute Of Ultrasonic Instruments Co., Ltd. | Shantou Guangdong, China | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shantou Institute Of Ultrasonic Instruments Co., Ltd. | SHANTOU Guangdong, China | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Siemens Shanghai, Medical Equipment Ltd. | Shanghai, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| iRay Imaging Technology (Haining) Limited | Haining Zhejiang, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| iRay Imaging Technology Taicang Limited | Taicang Jiangsu, China | Contract 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.