Skip to the page

Data / Medical devices / Japan / IONIC Corporation

IONIC Corporation: FDA-registered device maker in Nagareyama Chiba, Japan, 1 510(k) clearance

IONIC Corporation is registered with the FDA (registration 8043931) in Nagareyama Chiba, Japan. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 4, 1994. Registered through 2027. 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.

FDA registration number
8043931
FEI number
4803
Address
914-1 Nazukari, Nagareyama Chiba, Japan, 270-0145
Owner or operator
IONIC Corporation (10023394)
Roles
Exporter to the US, Manufacturer
First device listed
November 21, 2007
Registered through
2027
Brand names listed
IONIC KISS, KISS YOU, KISS YOU IONPA, KISS YOU IONPA home, Smart KISS YOU, hyG, ionic

Devices it lists

DeviceProduct codeClassRoleSource
Toothbrush, Ionic, Battery-PoweredMMD1Exporter to the US, Manufactureraccessdata.fda.gov
Toothbrush, PoweredJEQ1Exporter to the US, Manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
March 4, 1994K915576HUBUKA HYG TOOTHBRUSHMMDSubstantially EquivalentHukuba Dental Corp.accessdata.fda.gov

Compare with other makers

Updated March 4, 1994. 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.