Wheelchair & Scooter Express: FDA filings under this applicant name

FDA lists 7 510(k) clearances under the applicant name “Wheelchair & Scooter Express” (first 2003, latest 2003), across 2 product codes in 1 review panel. Median 510(k) review time under this name: 121 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.

510(k) clearances per year

YearClearancesMedian review days
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Top product codes

Product codeDeviceSubmissions510(k) clearances
INIVehicle, Motorized 3-Wheeled44
ITIWheelchair, Powered33

Review panels

Most recent Wheelchair & Scooter Express 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K032441F-10 FOLDING POWER CHAIRITI2003-10-0660
K030757COACH 777-4INI2003-10-06209
K030756COACH 777-3INI2003-10-06209
K032440F-11 FOLDING POWER CHAIRITI2003-09-2347
K030758COACH 888INI2003-07-31142
K030760COACH 888WITI2003-07-10121
K030759LITTLE COACHINI2003-05-0151

Recalls

openFDA lists no recalls under a recalling firm named Wheelchair & Scooter Express.

Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.

Frequently asked questions

How many FDA 510(k) clearances are listed under Wheelchair & Scooter Express?

FDA lists 7 510(k) clearances under the applicant name “Wheelchair & Scooter Express” (first 2003, latest 2003), across 2 product codes in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.

How long has FDA taken to clear 510(k)s filed by Wheelchair & Scooter Express?

The median time from FDA receipt to decision across 510(k)s cleared under the name Wheelchair & Scooter Express is 121 days.

Which FDA product codes appear under Wheelchair & Scooter Express?

The most frequent FDA product codes under this applicant name are INI (Vehicle, Motorized 3-Wheeled, 4); ITI (Wheelchair, Powered, 3).

Next steps

Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.

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