510(k) Report

FDA applicant

Sensory Aids Corp.

Bensenville, IL4 decisions1986–19870 recalls

FDA records 4 decisions for Sensory Aids Corp. (Bensenville, IL) from 1986 to 1987: 4 510(k) clearances. Most are in product codes EWO (Audiometer) and ILQ (System, Communication, 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, ophthalmic panel, where it files most

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

FDA decisions per year

No FDA decision for Sensory Aids Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Sensory Aids Corp. 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?

  • EWOAudiometer1decision
  • ILQSystem, Communication, Powered1decision
  • HOTAid, Vision Image Intensification1decision
  • HPFAid, Vision, Electronic, Ac-Powered1decision

What has FDA decided for it lately?

  • K872042Playtone AudiometerSensory Aids Corp. · 1987
  • K863995KeynoteSensory Aids Corp. · 1986
  • K863994ViewscanSensory Aids Corp. · 1986
  • K863993VTS Reporter or VTS LinkSensory Aids Corp. · 1986

All 4 as Sensory Aids Corp. →