510(k) Report

FDA applicant

Davis Positioning Systems, Inc.

Burton, MI1 decision1989–19890 recalls

FDA records 1 decision for Davis Positioning Systems, Inc. (Burton, MI) in 1989: 1 510(k) clearance. All are in product code IPL (Wheelchair, Standup). 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 Davis Positioning Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Davis Positioning Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Davis Positioning Systems, Inc. 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?

  • IPLWheelchair, Standup1decision

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.

  • K890602Standing Dani WheelstandDavis Positioning Systems, Inc. · 19891cites it

What has FDA decided for it lately?

  • K890602Standing Dani WheelstandDavis Positioning Systems, Inc. · 1989

The one decision as Davis Positioning Systems, Inc. →

Other applicant names beginning “Davis”

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

Davis & Geck, Inc. 46Davis Schottlander & Davis, Ltd. 7Davis Lead Aprons, Inc. 3Davis Assoc. 1Davis Medical 1Davis-Smith Corp. 1