Data / Medical devices / Camera, Multi Format, Radiological
Camera, Multi Format, Radiological (LMC): 12 FDA-registered makers in 5 countries
12 establishments in 5 countries are registered with the FDA to make Camera, Multi Format, Radiological (product code LMC, Class 2, 21 CFR 892.2040). 7 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 121 510(k) clearances under this code, the latest on June 26, 2014, and lists 3 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- LMC
- Device class
- 2
- Regulation
- 892.2040
- Medical specialty
- Radiology
Makers by country
| Country | Makers |
|---|---|
| Japan | 5 |
| United States | 3 |
| China | 2 |
| Belgium | 1 |
| Germany | 1 |
Makers of Camera, Multi Format, Radiological
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 | 3 | October 25, 2007 | 0 | 0 | 0 | api.fda.gov |
| Agfa-Gevaert Healthcare GMBH | PEISSENBERG Bavaria, Germany | Manufacturer | 3 | October 25, 2007 | 0 | 0 | 0 | api.fda.gov |
| Codonics, Inc. | Middleburg Heights, OH, United States | Complaint file establishment, Manufacturer, Remanufacturer | 2 | March 16, 2006 | 0 | 0 | 0 | api.fda.gov |
| Fujifilm Corporation | ASHIGARAKAMI-GUN Kanagawa, Japan | Complaint file establishment, Manufacturer | 2 | January 9, 2004 | 0 | 0 | 0 | api.fda.gov |
| FUJIFILM Imaging System (Suzhou) Co., Ltd. | Suzhou Jiangsu, China | Manufacturer | 2 | January 9, 2004 | 0 | 0 | 0 | api.fda.gov |
| Konica Minolta Technoproducts Co., Ltd. | SAYAMA-SHI Saitama, Japan | Manufacturer | 1 | July 1, 2008 | 0 | 0 | 0 | api.fda.gov |
| Konica Minolta, Inc. | HACHIOJI-SHI Tokyo, Japan | Specification developer | 1 | July 1, 2008 | 0 | 0 | 0 | api.fda.gov |
| Qisda Electronics (suzhou) Co., Ltd. | Suzhou Jiangsu, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Swemco | Moorestown, NJ, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sony Corporation | Yokohama-shi Kanagawa, Japan | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sony Global Manufacturing & Operations Corporation Kohda Site | Nukata-gun Aichi, Japan | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ZiphyCare, Inc. | New York, NY, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated June 26, 2014. 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.