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.
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- 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
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Electrode, Cutaneous | GXY | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Electrode, Needle | GXZ | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Electromyograph, Diagnostic | IKN | 2 | Contract manufacturer | accessdata.fda.gov |
| Full-Montage Standard Electroencephalograph | GWQ | 2 | Contract manufacturer | accessdata.fda.gov |
| Stimulator, Auditory, Evoked Response | GWJ | 2 | Contract manufacturer | accessdata.fda.gov |
| Stimulator, Electrical, Evoked Response | GWF | 2 | Contract manufacturer | accessdata.fda.gov |
| Stimulator, Nerve | ETN | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Stimulator, Photic, Evoked Response | GWE | 2 | Contract manufacturer | accessdata.fda.gov |
| System, Imaging, Pulsed Doppler, Ultrasonic | IYN | 2 | Contract manufacturer | accessdata.fda.gov |
| Transducer, Ultrasonic, Diagnostic | ITX | 2 | Contract manufacturer | accessdata.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.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| April 2, 2012 | K112426 | XIAN FRIENDSHIP DISPOSABLE NERVE STIMULATOR PROBES | ETN | Substantially Equivalent | Xian Friendship Medical Electronics Co., Ltd. | accessdata.fda.gov |
| August 30, 2011 | K110289 | FRIENDSHIP MEDICAL DISPOSABLE PRE-GELLED AG / AGCL SURFACE ELECTRODE | GXY | Substantially Equivalent | Xian Friendship Medical Electronics Co., Ltd. | accessdata.fda.gov |
| May 16, 2008 | K072276 | SUBDERMAL NEEDLE ELECTRODES | GXZ | Substantially Equivalent | Xian Friendship Electronics Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Electrode, Needle
- All makers of Stimulator, Nerve
- All makers of Stimulator, Electrical, Evoked Response
- All makers of Electromyograph, Diagnostic
- All makers of Electrode, Cutaneous
- All makers of Stimulator, Photic, Evoked Response
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.