FDA applicant

Associates IN Biofeedback

Walker, MI1 decision1980–19800 recalls

FDA records 1 decision for Associates IN Biofeedback (Walker, MI) in 1980: 1 510(k) clearance. All are in product code HIR (Perineometer). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Associates IN Biofeedback’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Associates IN Biofeedback since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Associates”

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

Associates of Cape Cod, Inc. 2 Associates IN Radiology, Inc. 1

Associates IN Biofeedback

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Associates”