510(k) Report

FDA applicant

Kindel & Anderson

Mchenry, IL4 decisions1980–19820 recalls

FDA records 4 decisions for Kindel & Anderson (Mchenry, IL) from 1980 to 1982: 4 510(k) clearances. Most are in product codes ESD (Hearing Aid, Air-Conduction, Prescription) and LEZ (Aids, Speech Training For The Hearing Impaired…). 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, ear, nose and throat panel, where it files most

How often FDA has decided Kindel & Anderson’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Kindel & Anderson since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Kindel & Anderson 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?

  • ESDHearing Aid, Air-Conduction, Prescription2decisions
  • LEZAids, Speech Training For The Hearing Impaired (Ac-Powered And Patient-Contact)1decision
  • KHLHearing Aid, Master1decision

Who builds on its devices?

Later devices cite its devices 1 time; 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.

  • K802870Rion Electro-Palatograph Model DP-01Kindel & Anderson · 19801cites it

What has FDA decided for it lately?

  • K823383Hearing Aid HB-33 RionetKindel & Anderson · 1982
  • K823384Hearing Aid HB-72 RionetKindel & Anderson · 1982
  • K802870Rion Electro-Palatograph Model DP-01Kindel & Anderson · 1980
  • K802812Rionet Hearing AidKindel & Anderson · 1980

All 4 as Kindel & Anderson →