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Data / Medical devices / China / Suzhou Green Pine Medical Co., Ltd

Suzhou Green Pine Medical Co., Ltd: FDA-registered device maker in Suzhou City Jiangsu, China, 1 510(k) clearance

Suzhou Green Pine Medical Co., Ltd is registered with the FDA (registration 3043105518) in Suzhou City Jiangsu, China. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 23, 2026. 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
3043105518
Address
No.103, 1st Floor, Building 1, 338 Xinsheng Road, Huaqiao Town, Kunshan City, Suzhou City Jiangsu, China, 215300
Owner or operator
Suzhou Green Pine Medical Co., Ltd (10094605)
Roles
Contract manufacturer, Manufacturer
First device listed
December 10, 2025
Registered through
2026
Brand names listed
Electric wheelchair (GP100), Scooter Model R, WHILL Model C2

Devices it lists

DeviceProduct codeClassRoleSource
Vehicle, Motorized 3-WheeledINI2Contract manufactureraccessdata.fda.gov
Wheelchair, PoweredITI2Contract manufacturer, Manufactureraccessdata.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
September 23, 2026K262582Electric wheelchair (GP100)ITISubstantially EquivalentSuzhou Green Pine Medical Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated September 23, 2026. 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.