Skip to the page

Data / Medical devices / Japan / Machida Endoscope Co., Ltd.

Machida Endoscope Co., Ltd.: FDA-registered device maker in Abiko Chiba, Japan, 1 510(k) clearance

Machida Endoscope Co., Ltd. is registered with the FDA (registration 9681246) in Abiko Chiba, Japan. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 13, 1982. Registered through 2026. 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
9681246
FEI number
3002807522
Address
15-12 Abiko 1 Chome, Abiko Chiba, Japan, 270-1166
Owner or operator
MACHIDA ENDOSCOPE CO., LTD. (9020972)
Roles
Manufacturer
First device listed
August 12, 2001
Registered through
2026
Brand names listed
MACHIDA

Devices it lists

DeviceProduct codeClassRoleSource
Laryngoscope, NasopharyngoscopeEQN2Manufactureraccessdata.fda.gov
Laryngoscope, RigidCCW1Manufactureraccessdata.fda.gov
Led Light SourceNTN2Manufactureraccessdata.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
May 13, 1982K821182MODEL ENT-4L-FLEXIBLE NASOPHARYNGO-EQNSubstantially EquivalentMachida America, Inc.accessdata.fda.gov

Compare with other makers

Updated May 13, 1982. 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.