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Data / Medical devices / China / Weifang KM Electronics Co., Ltd

Weifang KM Electronics Co., Ltd: FDA-registered device maker in Weifang Shandong, China, 1 510(k) clearance

Weifang KM Electronics Co., Ltd is registered with the FDA (registration 3010273372) in Weifang Shandong, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated April 15, 2019. 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
3010273372
Address
Building 2, No. 189 Shengrui Street, Zhuodao Community Qingchi Sub-district Office, Weifang High-tech Zone, Weifang Shandong, China, 261000
Owner or operator
Weifang KM Electronics Co., LTD (10060343)
Roles
Manufacturer
First device listed
May 9, 2019
Registered through
2026
Brand names listed
Powered laser surgical instrument

Devices it lists

DeviceProduct codeClassRoleSource
Powered Laser Surgical InstrumentGEX2Manufactureraccessdata.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
April 15, 2019K182924Diode Laser Treatment SystemGEXSubstantially EquivalentWeifang KM Electronics Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated April 15, 2019. 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.