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Data / Medical devices / China / menovex Medical Technology (Shenzhen) Co., Ltd

menovex Medical Technology (Shenzhen) Co., Ltd: FDA-registered device maker in Shenzhen Guangdong, China, 1 510(k) clearance

menovex Medical Technology (Shenzhen) Co., Ltd is registered with the FDA (registration 3042262496) in Shenzhen Guangdong, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 4, 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
3042262496
Address
401, 501, Building 13, Biomedicine Innovation Industrial Park, No. 14, Jinhui Road Jinsha Community, Kengzi Street, Pingshan District, Shenzhen Guangdong, China, 518118
Owner or operator
menovex Medical Technology (Shenzhen) Co., Ltd (10094241)
Roles
Manufacturer
First device listed
December 3, 2025
Registered through
2026
Brand names listed
tamburo Thulium Fiber Laser System, tamburo Thulium Laser Fiber

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
November 4, 2025K251303Tamburo Thulium Fiber Laser SystemGEXSubstantially EquivalentMenovex Medical Technology (Shenzhen) Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated November 4, 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.