Skip to the page

Data / Medical devices / South Korea / KP Trading Co., Ltd.

KP Trading Co., Ltd.: FDA-registered device maker in Hwaseong-si Gyeonggi, South Korea, 1 510(k) clearance

KP Trading Co., Ltd. is registered with the FDA (registration 3017405979) in Hwaseong-si Gyeonggi, South Korea. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 22, 2025. 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
3017405979
Address
21-7, Sandan-ro, 20 beon-gil, Danwon-gu, Ansan-si, Gyeonggi-do, Republic of Korea, Hwaseong-si Gyeonggi, South Korea, 18627
Owner or operator
KP Trading Co., Ltd. (10076231)
Roles
Exporter to the US, Manufacturer
First device listed
January 8, 2026
Registered through
2026
Brand names listed
Always KF-AD, Always KF94, Always KPT95, KP Protective Face Mask

Devices it lists

DeviceProduct codeClassRoleSource
Mask, SurgicalFXX2Exporter 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
December 22, 2025K243342KP Protective Face MaskFXXSubstantially EquivalentKp Trading Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated December 22, 2025. 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.