Data / Medical devices / Illuminator, Radiographic-Film
Illuminator, Radiographic-Film (IXC): 16 FDA-registered makers in 6 countries
16 establishments in 6 countries are registered with the FDA to make Illuminator, Radiographic-Film (product code IXC, Class 1, 21 CFR 892.1890). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 18 510(k) clearances under this code, the latest on June 1, 1999, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- IXC
- Device class
- 1
- Regulation
- 892.1890
- Medical specialty
- Radiology
Makers by country
| Country | Makers |
|---|---|
| China | 6 |
| United States | 4 |
| Canada | 2 |
| India | 2 |
| Taiwan | 1 |
| Germany | 1 |
Makers of Illuminator, Radiographic-Film
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Ari Medical Technology Co., Ltd. | Hefei Anhui, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Beyes Dental Inc | Toronto Ontario, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| CPAC Equipment, Inc. | Leicester, NY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Danyang New Hope Medical Equipment Co., Ltd | Danyang Jiangsu, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dentsply LLC | York, PA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dhef Inc. | New Taipei City, Taiwan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Galaxy India | New Delhi, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Guangdong Yuehua Medical Instrument Factory Co., Ltd. | Shantou Guangdong, China | Contract manufacturer, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hefei MT Medical Co.,ltd. | Hefei Anhui, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Innovative Medical Products, Inc. | Plainville, CT, United States | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Inspital Medical Technology GMBH | Neuss North Rhine-Westphalia, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jiangsu Keling Medical Appliances Co.,ltd. | Yangzhou Jiangsu, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lakong Medical Devices Co., Ltd. | Dongguan Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Onvet Medical Canada Inc | TORONTO Ontario, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Staan Biomed Engineering Private Limited | COIMBATORE Tamil Nadu, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Wolf X-Ray Corp | Battleboro, NC, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov |
Updated June 1, 1999. 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.