510(k) Report

FDA applicant

American Invalift Corp.

White Plains, NY1 decision1992–19920 recalls

FDA records 1 decision for American Invalift Corp. (White Plains, NY) in 1992: 1 510(k) clearance. All are in product code FRZ (Device, Patient Transfer, 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, general hospital panel, where it files most

How often FDA has decided American Invalift Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for American Invalift Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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Which product codes does it file in?

  • FRZDevice, Patient Transfer, Powered1decision

What has FDA decided for it lately?

  • K910830InvaliftAmerican Invalift Corp. · 1992

The one decision as American Invalift Corp. →