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Data / Medical devices / Wheelchair, Standup

Wheelchair, Standup (IPL): 14 FDA-registered makers in 9 countries

14 establishments in 9 countries are registered with the FDA to make Wheelchair, Standup (product code IPL, Class 2, 21 CFR 890.3900). 13 of them have a 510(k) clearance or PMA approval on file and 1 has a recall event. The FDA has issued 66 510(k) clearances under this code, the latest on March 12, 2025, and lists 1 recall event (0 Class I). 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.

Get every maker of this deviceMakers in the United StatesWatch this device
Product code
IPL
Device class
2
Regulation
890.3900
Medical specialty
Physical Medicine

Makers by country

CountryMakers
United States6
Switzerland1
Sweden1
Taiwan1
Canada1
Germany1
China1
Israel1
Australia1

Makers of Wheelchair, Standup

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Levo AGWOHLEN Aargau, SwitzerlandManufacturer3October 24, 2008000api.fda.gov
ATZ ManufacturingMarshall, MN, United StatesManufacturer2February 10, 2022000api.fda.gov
Matia Robotics (us), Inc.Salt Lake City, UT, United StatesManufacturer2May 29, 2020000api.fda.gov
Permobil ABSundsvall Vasternorrland, SwedenSpecification developer2February 27, 2020000api.fda.gov
Permobil, Inc.Lebanon, TN, United StatesManufacturer2February 27, 2020000api.fda.gov
The Standing CompanySaginaw, MI, United StatesManufacturer2January 22, 2004010api.fda.gov
E-Teng Technology Inc.New Taipei City, TaiwanContract manufacturer, Manufacturer1August 9, 2013000api.fda.gov
Motion Concepts LPVaughan Ontario, CanadaManufacturer1August 13, 2019000api.fda.gov
Powerbase Tec GMBHGieboldehausen, Niedersachsen Lower Saxony, GermanyManufacturer1January 21, 2022000api.fda.gov
Shenzhen Zuowei Technology Co.,ltd.Shenzhen Guangdong, ChinaManufacturer1March 12, 2025000api.fda.gov
Sunrise Medical (us) LLCFresno, CA, United StatesComplaint file establishment, Specification developer1January 16, 2018000api.fda.gov
Sunrise Medical (US) LLCMount Juliet, TN, United StatesComplaint file establishment, Manufacturer1January 16, 2018000api.fda.gov
Upnride Robotics LtdYokneam Illit Northern, IsraelManufacturer1September 12, 2019000api.fda.gov
Magic MobilityScoresby Victoria, AustraliaComplaint file establishment, Manufacturer0000api.fda.gov

Updated March 12, 2025. 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.