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Data / Medical devices / China / Zhuhai Wesee Meditech Co., Ltd

Zhuhai Wesee Meditech Co., Ltd: FDA-registered device maker in Zhuhai Guangdong, China, 1 510(k) clearance

Zhuhai Wesee Meditech Co., Ltd is registered with the FDA (registration 3045010519) in Zhuhai Guangdong, China. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 25, 2026. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3045010519
Address
3-301, 178 Dingxing Road, Tangjiawan Town, Hitech Zone, Zhuhai Guangdong, China, 519085
Owner or operator
Zhuhai Wesee Meditech Co., Ltd (10095636)
Roles
Manufacturer
First device listed
April 7, 2026
Registered through
2026
Brand names listed
Q202D Disposable Video Laryngoscope, SP11A Disposable Video Rhinolaryngscope

Devices it lists

DeviceProduct codeClassRoleSource
Laryngoscope, RigidCCW1Manufactureraccessdata.fda.gov
Nasopharyngoscope (Flexible Or Rigid)EOB2Manufactureraccessdata.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
March 25, 2026K253184Video Rhinolaryngoscope System (Disposable Video Rhinolaryngoscope SP11A Endoscopic Video Processor M110B)EOBSubstantially EquivalentZhuhai Wesee Meditech Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated March 25, 2026. 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.