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Data / Medical devices / China / Yunbo Times (taizhou) Technology Co. Ltd.

Yunbo Times (taizhou) Technology Co. Ltd.: FDA-registered device maker in Taizhou Zhejiang, China, 2 510(k) clearances

Yunbo Times (taizhou) Technology Co. Ltd. is registered with the FDA (registration 3031885960) in Taizhou Zhejiang, China. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated November 18, 2021. Registered through 2026. FDA data exported November 3, 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
3031885960
Address
Shangshan Industrial Park, Gaoqiao, Huangyan, Taizhou Zhejiang, China, 318020
Owner or operator
Yunbo Times (Taizhou) Technology Co. Ltd. (10095907)
Roles
Exporter to the US
First device listed
May 20, 2026
Registered through
2026

Devices it lists

DeviceProduct codeClassRoleSource
Lubricant, PersonalNUC2Exporter to the USaccessdata.fda.gov
Pad, Menstrual, UnscentedHHD1Exporter 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
November 18, 2021K212104Water-soluble Personal LubricantNUCSubstantially EquivalentFoshan Pingchuang Medical Technology Co., Ltd.accessdata.fda.gov
May 18, 2021K202667Personal Lubricant JellyNUCSubstantially EquivalentNantong Health & Beyond Hygienic Products, Inc.accessdata.fda.gov

Compare with other makers

Updated November 18, 2021. 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.