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Data / Medical devices / China / Xian Friendship Medical Electronics Co., Ltd.

Xian Friendship Medical Electronics Co., Ltd.: FDA-registered device maker in Xi'an Shaanxi, China, 3 510(k) clearances

Xian Friendship Medical Electronics Co., Ltd. is registered with the FDA (registration 3003851073) in Xi'an Shaanxi, China. It lists 10 device types. The FDA files 3 510(k) clearances under its listings, the newest dated April 2, 2012. 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
3003851073
Address
No.9 Gao Xin 1st Road, High-Tech Development Zone, Xi'an Shaanxi, China, 710075
Owner or operator
Xian Friendship Medical Electronics Co., Ltd. (9053765)
Roles
Contract manufacturer, Manufacturer
First device listed
December 4, 2007
Registered through
2026
Brand names listed
Cadwell Industries Inc., Friendship Medical, Medtronic, Sunspots

Devices it lists

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
April 2, 2012K112426XIAN FRIENDSHIP DISPOSABLE NERVE STIMULATOR PROBESETNSubstantially EquivalentXian Friendship Medical Electronics Co., Ltd.accessdata.fda.gov
August 30, 2011K110289FRIENDSHIP MEDICAL DISPOSABLE PRE-GELLED AG / AGCL SURFACE ELECTRODEGXYSubstantially EquivalentXian Friendship Medical Electronics Co., Ltd.accessdata.fda.gov
May 16, 2008K072276SUBDERMAL NEEDLE ELECTRODESGXZSubstantially EquivalentXian Friendship Electronics Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated April 2, 2012. 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.