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Data / Medical devices / United States / Us Shipcell Technology Inc

Us Shipcell Technology Inc: FDA-registered device maker in Montclair, CA, United States, 1 510(k) clearance

Us Shipcell Technology Inc is registered with the FDA (registration 3042501731) in Montclair, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated September 22, 2023. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3042501731
Address
5161 Richton St, Montclair, CA, United States, 91763
Owner or operator
US SHIPCELL TECHNOLOGY INC (10094694)
Roles
Specification developer
First device listed
December 16, 2025
Registered through
2026
Brand names listed
Electric Wheelchair

Devices it lists

DeviceProduct codeClassRoleSource
Wheelchair, PoweredITI2Specification developeraccessdata.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 22, 2023K232193Electrically Power Wheelchairs (Models:YLB-W-0812-A01, YLB-W-0812-A02, YLB-W-0812-A03)ITISubstantially EquivalentYurob Rehabilitation Medical Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated September 22, 2023. 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.