Data / Medical devices / Display, Diagnostic Radiology / China
FDA-registered makers of Display, Diagnostic Radiology in China: 5 establishments
5 establishments in China are registered with the FDA to make Display, Diagnostic Radiology (product code PGY). 4 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
- Display, Diagnostic Radiology
- Product code
- PGY
- Country
- China
Makers of Display, Diagnostic Radiology in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Nanjing Jusha Display Technology Co., Ltd | Nanjing Jiangsu, China | Manufacturer | 15 | June 9, 2023 | 0 | 0 | 0 | api.fda.gov |
| LG Electronics Nanjing New Technology Co., Ltd. | Nanjing Jiangsu, China | Exporter to the US, Manufacturer | 11 | June 12, 2026 | 0 | 0 | 0 | api.fda.gov |
| Qingdao Hisense Medical Equipment Co.,Ltd. | Qingdao Shandong, China | Manufacturer | 3 | November 17, 2022 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Beacon Display Technology Co., Ltd. | Shenzhen Guangdong, China | Complaint file establishment, Manufacturer | 3 | October 29, 2025 | 0 | 0 | 0 | api.fda.gov |
| Barco (Suzhou) Healthcare Technology Co., Ltd. | Suzhou 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.