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Data / Medical devices / South Korea / Medicon Co., Ltd.

Medicon Co., Ltd.: FDA-registered device maker in Wonju Gangwon, South Korea, 1 510(k) clearance

Medicon Co., Ltd. is registered with the FDA (registration 3009862779) in Wonju Gangwon, South Korea. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated February 29, 2012. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3009862779
Address
Rm 506, 200 Gieopdosi-ro, Jijeong-myeon, Wonju Gangwon, South Korea, 26354
Owner or operator
MEDICON CO., LTD. (10075825)
Roles
Manufacturer
First device listed
June 27, 2020
Registered through
2026
Brand names listed
CLEANE / CLEANE POP, CLEANE+, KATIE YOUNG CLEANE, TWAVE

Devices it lists

DeviceProduct codeClassRoleSource
Massager, Therapeutic, ElectricISA1Manufactureraccessdata.fda.gov
Over The Counter Thermal Treatment For Acne.OZC2Manufactureraccessdata.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
February 29, 2012K111341CLEANE / CLEANE POPOZCSubstantially EquivalentMedicon Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated February 29, 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.