Data / Medical devices / Holder, Radiographic Cassette, Wall-Mounted
Holder, Radiographic Cassette, Wall-Mounted (IXY): 30 FDA-registered makers in 10 countries
30 establishments in 10 countries are registered with the FDA to make Holder, Radiographic Cassette, Wall-Mounted (product code IXY, Class 1, 21 CFR 892.1880). 0 of them have a 510(k) clearance or PMA approval on file and 1 has a recall event. The FDA has issued 21 510(k) clearances under this code, the latest on August 11, 1995, and lists 4 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- IXY
- Device class
- 1
- Regulation
- 892.1880
- Medical specialty
- Radiology
Makers by country
| Country | Makers |
|---|---|
| United States | 9 |
| China | 6 |
| South Korea | 5 |
| Germany | 3 |
| Sweden | 2 |
| Belgium | 1 |
| Mexico | 1 |
| United Kingdom | 1 |
| Spain | 1 |
| Japan | 1 |
Makers of Holder, Radiographic Cassette, Wall-Mounted
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 |
|---|---|---|---|---|---|---|---|---|
| Agfa N.V. | Mortsel Antwerpen, Belgium | Complaint file establishment, Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Aktina Medical Corp. | Congers, NY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Arcoma AB | VAXJO Kronoberg, Sweden | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Accogent Pausch | Eatontown, NJ, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Carestream Health, Inc., Global R&D Center | Shanghai, China | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Compania Mexicana De Radiologia CGR, S.A. De C.V. | Queretaro, Mexico | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Core Labs, LLC. | Englewood, CO, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Del Medical, Inc. | Bloomingdale, IL, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 1 | 0 | api.fda.gov | |
| DK Medical Systems Co., Ltd. | Pyeongtaek-si Gyeonggi, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dongguan Wanjin Industrial Co., Ltd | DongGuang Guangdong, China | Remanufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Drgem Corporation | Gwangmyeong-si Gyeongbuk, South Korea | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| DRGEM Corporation (Gimcheon Factory) | Gimcheon-si Gyeongbuk, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| DRTECH Corporation | Seongnam-si Gyeonggi, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ge Hangwei Medical Systems Co., Ltd. | Beijing, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| GE Healthcare (China) Co., Ltd. | Beijing, China | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jinyuan Medical Equipment(tianjin)co.,ltd | Tianjin, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kenex (electro-Medical) Ltd. | HARLOW Essex, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Livermoretech,inc | Plano, TX, United States | Manufacturer, Remanufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Marketlab Incorporated | Caledonia, MI, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| PAUSCH Medical GmbH | ERLANGEN Bavaria, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Philips Medical Systems DMC GmbH | Hamburg, Germany | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| RCI Operating CO LLC | Hilton, NY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Reina Imaging | Crystal Lake, IL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sedecal S.A. | ALGETE Madrid(Province), Spain | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shimadzu Corporation Medical Systems Division | Kyoto, Japan | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shinyoung For M Co., Ltd. | Namyangju-si Gyeonggi, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Siemens Shanghai, Medical Equipment Ltd. | Shanghai, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Solutions For Tomorrow AB | Vackelsang Kronoberg, Sweden | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Summit Industries, LLC | Niles, IL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Siemens Healthineers AG | KEMNATH Bavaria, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated August 11, 1995. 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.