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Data / Medical devices / China / Wuhu Snnda Medical Treatment Appliance Technology Co. Ltd.

Wuhu Snnda Medical Treatment Appliance Technology Co. Ltd.: FDA-registered device maker in Wuhu Anhui, China, 2 510(k) clearances

Wuhu Snnda Medical Treatment Appliance Technology Co. Ltd. is registered with the FDA (registration 3012936366) in Wuhu Anhui, China. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated June 25, 2013. 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
3012936366
Address
4F Overseas Student Pioneer Park, Science Innovation Centre Economic & Technological Development Zone North Yinhu Rd, Wuhu Anhui, China, 241007
Owner or operator
Wuhu Snnda Medical Treatment Appliance Technology Co. Ltd. (10057137)
Roles
Manufacturer
First device listed
February 27, 2018
Registered through
2026
Brand names listed
Shang Ring

Devices it lists

DeviceProduct codeClassRoleSource
Clamp, CircumcisionHFX2Manufactureraccessdata.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
June 25, 2013K131373SHANGRINGHFXSubstantially EquivalentWuhu Snnda Medical Treatment Appliance Technologyaccessdata.fda.gov
August 3, 2012K121789SHANGRINGHFXSubstantially EquivalentWuhu Snna Medical Treatment Appliance Technology Caccessdata.fda.gov

Compare with other makers

Updated June 25, 2013. 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.