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Data / Medical devices / Japan / Narishige Lifemed Co., Ltd

Narishige Lifemed Co., Ltd: FDA-registered device maker in Tokyo, Japan, 7 510(k) clearances

Narishige Lifemed Co., Ltd is registered with the FDA (registration 3012789229) in Tokyo, Japan. It lists 1 device type. The FDA files 7 510(k) clearances under its listings, the newest dated June 20, 2012. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3012789229
Address
13-12 Kyuden 3-chome Setagaya-ku, Tokyo, Japan, 157-0064
Owner or operator
NARISHIGE INTERNATIONAL USA, INC. (9041765)
Roles
Manufacturer
First device listed
December 13, 2007
Registered through
2026
Brand names listed
IM-11 Pneumatic Microinjector, IM-11-2VM, IM-12VM, IM-21VM, IM-9B Microinjector, IM-9BVM, IM-9C Microinjector, IM-9CVM and more

Devices it lists

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
June 20, 2012K120877MICROMANIPULATOR SETMQJSubstantially EquivalentNarishige Co., Ltd.accessdata.fda.gov
March 15, 2012K113712IM-11 PNEUMATIC MICROINJECTORMQJSubstantially EquivalentNarishige Co., Ltd.accessdata.fda.gov
March 16, 2001K010298MN-4 COARSE MANIPULATORMQJSubstantially EquivalentNarishige Co., Ltd.accessdata.fda.gov
September 22, 2000K002659MMO-202ND THREE-AXIS HANGING JOYSTICK OIL HYDRAULIC MICROMANPULATORMQJSubstantially EquivalentNarishige Co., Ltd.accessdata.fda.gov
September 13, 2000K002291MOTOR-DRIVE MANIPULATOR MM-89MQJSubstantially EquivalentNarishige Co., Ltd.accessdata.fda.gov
July 7, 2000K001912IM-9B MICROINJECTORSMQJSubstantially EquivalentNarishige Co., Ltd.accessdata.fda.gov
July 7, 2000K001910IM-9C MICROINJECTORSMQJSubstantially EquivalentNarishige Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated June 20, 2012. 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.