Data / Medical devices / Grid, Radiographic
Grid, Radiographic (IXJ): 14 FDA-registered makers in 9 countries
14 establishments in 9 countries are registered with the FDA to make Grid, Radiographic (product code IXJ, Class 1, 21 CFR 892.1910). 1 of them has a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 15 510(k) clearances under this code, the latest on June 13, 1997, and lists 1 recall event (0 Class I). FDA data exported November 2, 2026.
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- Product code
- IXJ
- Device class
- 1
- Regulation
- 892.1910
- Medical specialty
- Radiology
Makers by country
| Country | Makers |
|---|---|
| United States | 4 |
| South Korea | 2 |
| Germany | 2 |
| Belgium | 1 |
| China | 1 |
| India | 1 |
| Japan | 1 |
| Italy | 1 |
| Netherlands | 1 |
Makers of Grid, Radiographic
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 |
|---|---|---|---|---|---|---|---|---|
| JPI Healthcare Co., Ltd | Seoul, South Korea | Manufacturer | 1 | January 20, 1995 | 0 | 0 | 0 | api.fda.gov |
| Agfa N.V. | Mortsel Antwerpen, Belgium | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Beekley Corporation | Bristol, CT, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Carestream Health, Inc | Rochester, NY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Del Medical, Inc. | Bloomingdale, IL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Guangzhou Bioway Medical Technology Joint-Stock Co.,ltd. | Guangzhou Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kiran Medical Systems A Div of Trivitron Healthcare Pvt. Ltd | Navi Mumbai Maharashtra, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mitaya MFG. Co., Ltd. | Kawagoe-shi Saitama, Japan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Orthofix SRL | BUSSOLENGO Verona, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Philips Medical Systems Nederland B.V. | BEST Noord-Brabant, Netherlands | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Philips Medical Systems DMC GmbH | Hamburg, Germany | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Soyee Product, Inc. | KANGNAM-KU, SEOUL Gyeonggi, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Siemens Healthineers AG | ERLANGEN Bavaria, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Webb Medical | Phila, PA, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated June 13, 1997. 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.