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Data / Medical devices / China / Shenzhen Upnmed Equipment Co., Ltd.

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

Shenzhen Upnmed Equipment Co., Ltd. is registered with the FDA (registration 3042119591) in Shenzhen Guangdong, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 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
3042119591
Address
No.301,Building #41st,The 3rd Industrial Zone,Xitian Community,Gongming Street,Guangming District, Shenzhen Guangdong, China, 518000
Owner or operator
Shenzhen Upnmed Equipment Co., Ltd. (10096254)
Roles
Exporter to the US, Manufacturer
First device listed
August 8, 2026
Registered through
2026
Brand names listed
SpO2 Sensor

Devices it lists

DeviceProduct codeClassRoleSource
OximeterDQA2Exporter 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
May 15, 2019K183277SpO2 SensorDQASubstantially EquivalentShenzhen Upnmed Equipment Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated May 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.