FDA applicant

Bruno Independent Living Aids, Inc.

Oconomowoc, WI12 decisions1992–20120 recalls

FDA records 12 decisions for Bruno Independent Living Aids, Inc. (Oconomowoc, WI) from 1992 to 2012: 12 510(k) clearances. Most are in product codes ILK (Transport, Patient, Powered) and 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 Bruno Independent Living Aids, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2012

2007high 1 (2012) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Bruno Independent Living Aids, Inc.’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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Other applicant names beginning “Bruno”

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

Bruno Vision Care, LLC 2

Bruno Independent Living Aids, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Bruno”