Skip to the page

Data / Medical devices / System, Digital Image Communications, Radiological / Taiwan

FDA-registered makers of System, Digital Image Communications, Radiological in Taiwan: 7 establishments

7 establishments in Taiwan are registered with the FDA to make System, Digital Image Communications, Radiological (product code LMD). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Device
System, Digital Image Communications, Radiological
Product code
LMD
Country
Taiwan

Makers of System, Digital Image Communications, Radiological in Taiwan

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Acula Technology CorpLuchu Taoyuan, TaiwanManufacturer0000api.fda.gov
AsusTaipei City, TaiwanSpecification developer0000api.fda.gov
Daikso Co., Ltd.Guishan Dist., Taoyuan, TaiwanForeign private label distributor, Manufacturer0000api.fda.gov
Diva Laboratories, Ltd.New Taipei City, Taipei-District, 235, TaiwanManufacturer0000api.fda.gov
Ebm Technologies, Inc.Taipei, TaiwanManufacturer0000api.fda.gov
Medimaging Integrated Solution Inc.Hsinchu Hsinchu(City), TaiwanContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Taiwan Main Orthopaedic Biotechnology Co., LtdTaichung City, TaiwanManufacturer0000api.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.