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Data / Medical devices / Device, Digital Image Storage, Radiological / Japan

FDA-registered makers of Device, Digital Image Storage, Radiological in Japan: 8 establishments

8 establishments in Japan are registered with the FDA to make Device, Digital Image Storage, Radiological (product code LMB). 1 has 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
Device, Digital Image Storage, Radiological
Product code
LMB
Country
Japan

Makers of Device, Digital Image Storage, Radiological in Japan

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Sony CorporationYokohama-shi Kanagawa, JapanComplaint file establishment, Specification developer1July 3, 1996000api.fda.gov
Canon Components, Inc.KODAMA-GUN Saitama, JapanManufacturer0000api.fda.gov
Canon Inc.Kawasaki Kanagawa, JapanSpecification developer0000api.fda.gov
Canon.IncOHTA-KU Tokyo, JapanSpecification developer0000api.fda.gov
Eizo CorporationHAKUSAN Ishikawa, JapanManufacturer0000api.fda.gov
Sord CorporationChiba-Shi Tokyo, JapanContract manufacturer0000api.fda.gov
Sony Global Manufacturing & Operations Corporation Kohda SiteNukata-gun Aichi, JapanContract manufacturer0000api.fda.gov
Teac Manufacturing Solutions CorporationOME-SHI Tokyo, JapanManufacturer0000api.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.