Skip to the page

Data / Medical devices / China / Shenzhen Yashunmei Technology Co., Ltd.

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

Shenzhen Yashunmei Technology Co., Ltd. is registered with the FDA (registration 3044571218) in Shenzhen Guangdong, China. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 30, 1993. 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
3044571218
Address
No. 33 Yunfeng Road (No. 1 Huaque Road), Taoyuan Community, Dalang Street, Longhua District, Shenzhen Guangdong, China, 518110
Owner or operator
Shenzhen Yashunmei Technology Co., Ltd. (10095764)
Roles
Exporter to the US, Manufacturer
First device listed
April 26, 2026
Registered through
2026
Brand names listed
VRWCTNIY Portable Nebulizer Compressor Air Portable YS30 YS37 YS34E

Devices it lists

DeviceProduct codeClassRoleSource
Compressor, Air, PortableBTI2Manufactureraccessdata.fda.gov
Kit, Surgical Instrument, DisposableKDD1Exporter to the USaccessdata.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
September 30, 1993K931015DEVILBISS MODEL 4650 COMPRESSOR NEUBULIZERBTISubstantially EquivalentDevilbiss Health Care, Inc.accessdata.fda.gov

Compare with other makers

Updated September 30, 1993. 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.