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Data / Medical devices / South Korea / Jung Rim Medical Industrial Co., Ltd.

Jung Rim Medical Industrial Co., Ltd.: FDA-registered device maker in JINCHEON-GUN Chungbuk, South Korea, 1 510(k) clearance

Jung Rim Medical Industrial Co., Ltd. is registered with the FDA (registration 3004054016) in JINCHEON-GUN Chungbuk, South Korea. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 12, 2013. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number
3004054016
Address
187, Jinkwang-ro, Iwol-myeon, JINCHEON-GUN Chungbuk, South Korea, 27819
Owner or operator
JUNG RIM MEDICAL INDUSTRIAL CO., LTD. (10040881)
Roles
Manufacturer
First device listed
April 24, 2014
Registered through
2026
Brand names listed
PISTON SYRINGE

Devices it lists

DeviceProduct codeClassRoleSource
Needle, Hypodermic, Single LumenFMI2Manufactureraccessdata.fda.gov
Syringe, PistonFMF2Manufactureraccessdata.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
September 12, 2013K124037JUNG RIM SINGLE USE HYPODERMIC SYRINGE WITH NEEDLEFMFSubstantially EquivalentJung Rim Medical Industrial Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated September 12, 2013. 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.