Skip to the page

Data / Medical devices / China / Kunshan Aoshida Electric Technology Co., Ltd.

Kunshan Aoshida Electric Technology Co., Ltd.: FDA-registered device maker in Kunshan City Jiangsu, China, 1 510(k) clearance

Kunshan Aoshida Electric Technology Co., Ltd. is registered with the FDA (registration 3011969521) in Kunshan City Jiangsu, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 5, 2017. 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
3011969521
Address
No.6 Huanlou Road, Development Zone, Kunshan City Jiangsu, China, 215300
Owner or operator
Kunshan Aoshida Electric Technology Co., Ltd. (10054979)
Roles
Manufacturer
First device listed
May 19, 2017
Registered through
2026
Brand names listed
A04, A05, A07, A08C, A08CL, A05(T3), A08C(DE08), A08CL(DE08L), A11, A12, A12S A13, A15, D05, DE09, GT13, A06, A06L, A08L, A08, A09, A10, Power Wheelchair

Devices it lists

DeviceProduct codeClassRoleSource
Wheelchair, PoweredITI2Manufactureraccessdata.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 5, 2017K163204A08 Power wheelchairITISubstantially EquivalentKunshan Aoshida Electric Technology Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated May 5, 2017. 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.