FDA applicant

Independent Living, Inc.

Northfield, IL1 decision1985–19850 recalls

FDA records 1 decision for Independent Living, Inc. (Northfield, IL) in 1985: 1 510(k) clearance. All are in product code IQA (System, Environmental Control, 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 Independent Living, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Independent Living, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Other applicant names beginning “Independent”

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

Independent Transfer Equipment Co. 2 Independent Scintilation Imaging Systems, Inc. 1

Independent Living, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Independent”