510(k) Report

FDA applicant

Natural Access

Honolulu, HI1 decision1995–19950 recalls

FDA records 1 decision for Natural Access (Honolulu, HI) in 1995: 1 510(k) clearance. All are in product code IOR (Wheelchair, Mechanical). 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 Natural Access’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Natural Access since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • IORWheelchair, Mechanical1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K954261Landeez All-Terrain WheelchairNatural Access · 19951cites it

What has FDA decided for it lately?

  • K954261Landeez All-Terrain WheelchairNatural Access · 1995

The one decision as Natural Access →

Other applicant names beginning “Natural”

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

Natural Cycles Nordic AB 6Natural Technologies, Inc. 2The Natural Choice Co., Inc. 1Natural Herbal Products, Inc. 1Natural Energy Solutions AG 1