510(k) Report

FDA applicant

Permobil of America

Lexington, MA5 decisions1987–19870 recalls

FDA records 5 decisions for Permobil of America (Lexington, MA) in 1987: 5 510(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 Permobil of America’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Permobil of America since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Permobil of America 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?

  • ITIWheelchair, Powered5decisions

Who builds on its devices?

Later devices cite its devices 2 times; 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.

  • K870224Permobil MaxiorPermobil of America · 19871cites it
  • K870225Permobil ExteriorPermobil of America · 19871cites it

What has FDA decided for it lately?

  • K870227Permobil SuperiorPermobil of America · 1987
  • K870224Permobil MaxiorPermobil of America · 1987
  • K870228Permobil HexiorPermobil of America · 1987
  • K870226Permobil MiniorPermobil of America · 1987
  • K870225Permobil ExteriorPermobil of America · 1987

All 5 as Permobil of America →

Other applicant names beginning “Permobil”

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

Permobil AB 15