510(k) Report

FDA applicant

Excel Mobility Products, Inc.

Washington, DC2 decisions1992–19920 recalls

FDA records 2 decisions for Excel Mobility Products, Inc. (Washington, DC) in 1992: 2 510(k) clearances. All are in product code ITI (Wheelchair, Powered). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, physical medicine panel, where it files most

How often FDA has decided Excel Mobility Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Excel Mobility Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Excel Mobility Products, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Excel Mobility Products, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Which product codes does it file in?

  • ITIWheelchair, Powered2decisions

What has FDA decided for it lately?

  • K920325Rangeroller (Modified)Excel Mobility Products, Inc. · 1992
  • K915152RangerollerExcel Mobility Products, Inc. · 1992

All 2 as Excel Mobility Products, Inc. →

Other applicant names beginning “Excel”

FDA records each applicant name separately; these may or may not be the same firm.

Excel Tech., Ltd. 58Excel Scientific, Inc. 8Excel-Tech Ltd. (Xltek) 6Excel Medical, Inc. 5Excel Health Care Products 5Excel U.S.A. 3Excel Medical Products, Inc. 2Excel Rubber Products (M) Sdn. Bhd. 1Excel Medical Electronics, LLC 1Excel Porcelain Products 1Excel Glove Co., Ltd. 1Excel Medical Systems, Inc. 1