510(k) Report

FDA applicant

Patmont Motor Werks, Inc.

Minden, NV2 decisions2009–20100 recalls

FDA records 2 decisions for Patmont Motor Werks, Inc. (Minden, NV) from 2009 to 2010: 2 510(k) clearances. All are in product code IOR (Wheelchair, Mechanical). Its devices cite 4 predicates, 0 of them its own earlier devices. 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 Patmont Motor Werks, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2010

2009: 12010: 1
2009high 1 (2009) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2009.

FIG. 1 — Patmont Motor Werks, Inc. by year, 2009–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • IORWheelchair, Mechanical2decisions

Whose devices does it build on?

Its devices cite 4 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K102061Trevair Chair AdultPatmont Motor Werks, Inc. · 2010
  • K091478Trevair ChairPatmont Motor Werks, Inc. · 2009

All 2 as Patmont Motor Werks, Inc. →