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Data / Medical devices / Components, Wheelchair / United States

FDA-registered makers of Components, Wheelchair in the United States: 23 establishments

23 establishments in the United States are registered with the FDA to make Components, Wheelchair (product code KNN). 0 have a 510(k) clearance or PMA approval on file and 1 has a recall event. 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 makers of this device in the United StatesWatch these makers
Device
Components, Wheelchair
Product code
KNN
Country
United States

Makers of Components, Wheelchair in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
210 Innovations, LLCGroton, CT, United StatesManufacturer0000api.fda.gov
Broda Enterprises Usa Inc.Bonnie, UT, United StatesManufacturer0000api.fda.gov
Freedom Designs, Inc.Pharr, TX, United StatesComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
GUNNELL, Inc.Elk City, OK, United StatesManufacturer0000api.fda.gov
Invacare Corp. Dba Invacare AmericaN Ridgeville, OH, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Kalogon IncMelbourne, FL, United StatesManufacturer0000api.fda.gov
Ki MobilityStevens Point, WI, United StatesManufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Matrix Seating Usa, LLCNewberry, FL, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer0000api.fda.gov
Nova Ortho-Med, Inc.North Aurora, IL, United StatesSpecification developer0000api.fda.gov
Permobil, Inc.Lebanon, TN, United StatesContract manufacturer, Manufacturer, Repackager or relabeler0010api.fda.gov
Pride Mobility Products Corp.North Las Vegas, NV, United StatesManufacturer0000api.fda.gov
Pride Mobility Products Corp.Duryea, PA, United StatesManufacturer0000api.fda.gov
Pride Mobility Products CorporationNorth Las Vegas, NV, United StatesManufacturer0000api.fda.gov
Richardson Products, Inc.Frankfort, IL, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
ROHO, Inc.Belleville, IL, United StatesComplaint file establishment, Contract manufacturer, Manufacturer0000api.fda.gov
Stealth ProductsBurnet, TX, United StatesManufacturer0000api.fda.gov
Sunrise Medical (us) LLCFresno, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Seating DynamicsCentennial, CO, United StatesManufacturer0000api.fda.gov
Sunrise Medical (US) LLCMount Juliet, TN, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
The Comfort Companies, L.L.C.New Berlin, WI, United StatesManufacturer0000api.fda.gov
Tisport, LLCPasco, WA, United StatesManufacturer0000api.fda.gov
Tolt TechnologiesDuvall, WA, United StatesContract manufacturer, Manufacturer0000api.fda.gov

Updated November 2, 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.